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Cerapedics

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uuid0000mur

Namestring
Cerapedics
Legal namestring
Cerapedics Inc.
Websiteurl
cerapedics.com
Company typeenum
Private
Founded yearint
2015
Descriptiontext

Cerapedics is a privately-held commercial-stage medical device company headquartered in Westminster, Colorado, that develops and commercializes proprietary osteobiologic products for spinal fusion surgery. The company's core technology is the P-15 Osteogenic Cell Binding Peptide, a synthetic 15-amino-acid sequence derived from Type-1 collagen that is bound onto different osteoconductive scaffolds to accelerate bone formation through an attract-attach-activate mechanism. This technology is the basis for two FDA Premarket-Approved Class III drug-device combination products: i-FACTOR, approved in November 2015 for single-level anterior cervical discectomy and fusion (ACDF) and commercially launched in the U.S. in 2016, and PearlMatrix, approved in June 2025 for single-level transforaminal lumbar interbody fusion (TLIF) with expanded indications covering ALIF, PLIF, OLIF, and LLIF approved in January 2026. PearlMatrix is positioned as the first and only bone growth accelerator proven to accelerate lumbar fusion, backed by Level 1 clinical evidence from the ASPIRE IDE study (293 patients across 33 U.S. centers) and six-year i-FACTOR follow-up data showing 98.6% fusion rates.

Cerapedics generates revenue through direct hardware sales of bone graft products to hospitals and surgical centers, sold via a combination of direct sales representatives, local distribution partners, and group purchasing organization agreements with Premier Inc. and Vizient (the latter covering over 65% of U.S. acute care providers). International sales of i-FACTOR products are conducted through distributors, including Surgi-One in Canada, alongside CE Mark and TGA-listed products. The company serves spine surgeons and neurosurgeons performing cervical and lumbar fusion procedures, with named customers including Cleveland Clinic, Washington University School of Medicine, AdventHealth Avista, and Austin Brain and Spine. Pricing is not publicly disclosed, but products target the U.S. spinal bone graft substitution market, where approximately 465,000 fusion cases were performed in 2023.

The company employs approximately 250 people worldwide, has raised over $180 million cumulatively since 2007 across equity and debt rounds, and is led by Chairman and CEO Valeska Schroeder (appointed November 2022). KCK Group has been the lead institutional investor since a $22 million round in 2018, and the company is controlled by KCK Group as parent investor. The company has been recognized with industry awards including the 2018 MedTech Breakthrough Award for Best New Surgical Technology and Denver Post Top Workplaces in 2024 and 2026.

Short descriptiontext

Cerapedics is a Westminster, Colorado-based medical device company that develops and commercializes FDA PMA-approved P-15 peptide-enhanced bone graft products (i-FACTOR and PearlMatrix) for cervical and lumbar spinal fusion, sold to spine surgeons and hospitals through direct sales and GPO agreements with Premier Inc. and Vizient.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersWestminster, United States
HQ citystring
Westminster
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
bone graft substitutes, spinal fusion devices, osteobiologic products, peptide enhanced bone graft, spine surgery implants
Industry3 codes
1Bone Graft Substitutes & Orthobiologics (Synthetic/Allograft/DBM)
CodeHLAHAEAGPrimaryYes
2Tissue-Engineered Constructs & Scaffolds (natural/synthetic biomaterials)
CodeHLAAAGABPrimaryNo
3Spine Implants & Motion Preservation (Fusion/Disc/Interspinous)
CodeHLAHAEACPrimaryNo
NAICS code2 codes
  • Surgical Appliance and Supplies Manufacturing339113
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code2 codes
  • Orthopedic, Prosthetic & Surgical Appliances & Supplies3842
  • Biological Products, (No Disgnostic Substances)2836
Product category
Spinal Bone Graft Substitutes / Orthobiologics
Social media profiles2 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model3 records
1i-FACTOR Bone Graft
TypeHardware Sales
Description

FDA PMA-approved Class III drug-device combination product for single-level anterior cervical discectomy and fusion (ACDF). Commercialized since 2015/2016 in the U.S. market.

cerapedics.com
2PearlMatrix Bone Graft
TypeHardware Sales
Description

FDA PMA-approved Class III drug-device combination product for single-level transforaminal lumbar interbody fusion (TLIF). Approved June 2025 and now approved for expanded indications including ALIF, PLIF, OLIF, and LLIF approaches.

cerapedics.com
3International Products
TypeHardware Sales
Description

i-FACTOR products available internationally including i-FACTOR Putty and i-FACTOR Flex FR distributed through international markets. Products also available in Canada through distributor Surgi-One.

cerapedics.com
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels5 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Operations, Personnel, Marketing or Sales, Supply Chain
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1PearlMatrix
Description

P-15 Peptide Enhanced Bone Graft - FDA-approved Class III drug-device combination product for lumbar spine fusion (TLIF procedures). The first and only bone growth accelerator proven to accelerate lumbar fusion.

cerapedics.com
+1 more record
Core offering1 text field

Cerapedics develops, manufactures, and commercializes novel osteobiologic bone graft products based on its proprietary P-15 Osteogenic Cell Binding Peptide technology. The company sells FDA PMA-approved Class III drug-device combination products, including i-FACTOR for cervical spine fusion (ACDF) and PearlMatrix for lumbar spine fusion (TLIF, ALIF, PLIF, OLIF, LLIF), targeting spine surgeons and healthcare facilities worldwide.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • More than twice as many patients fused at six months vs. local autograft in TLIF procedures
+4 more records
Product and service5 records
1i-FACTOR P-15 Peptide Enhanced Bone Graft
CategorySpinal Bone Graft Substitute
Description

FDA PMA-approved Class III drug-device combination bone graft using P-15 Osteogenic Cell Binding Peptide technology for single-level anterior cervical discectomy and fusion (ACDF) procedures in patients with degenerative cervical disc disease. Has been used by surgeons since 2015/2016, with six-year IDE follow-up data showing 98.6% fusion rate. Targeted at spine surgeons seeking a clinically proven, cost-effective alternative to autograft for cervical fusion.

2PearlMatrix P-15 Peptide Enhanced Bone Graft
CategorySpinal Bone Graft Substitute
Description

FDA PMA-approved Class III drug-device combination bone graft using P-15 Osteogenic Cell Binding Peptide technology bound onto a flexible collagen matrix carrier. Indicated for single-level TLIF and now expanded for all major lumbar interbody surgical approaches (ALIF, PLIF, OLIF, LLIF). The first and only bone growth accelerator demonstrated to accelerate lumbar fusion in Level 1 IDE clinical data, with statistically superior time to fusion versus local autograft. Targeted at spine surgeons treating degenerative disc disease.

3i-FACTOR Flex FR
CategorySpinal Bone Graft Substitute
Description

Bone graft substitute utilizing P-15 Osteogenic Cell Binding Peptide technology with purified silk fibers as an inert carrier, providing enhanced cohesion, mechanical properties, and handling characteristics. Sterilized after packaging (terminally sterilized), stored at room temperature, with three-year shelf life, ready to use with no mixing or preparation. Distributed internationally.

4i-FACTOR Putty
CategorySpinal Bone Graft Substitute
Description

Bone graft substitute utilizing P-15 Osteogenic Cell Binding Peptide technology. Terminally sterilized after packaging, stored at room temperature, three-year shelf life, ready to use with no mixing or preparation required. Distributed internationally.

5i-FACTOR+ Matrix
CategorySpinal Bone Graft Substitute
Description

Next-generation P-15 Peptide Enhanced Bone Graft product approved by Health Canada, distributed in Canada through partner Surgi-One.

Scale indicator10 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2026-04-24
Description

Cerapedics announced a supplier agreement with Vizient, the nation's largest provider-driven healthcare performance improvement company, to distribute PearlMatrix P-15 Peptide Enhanced Bone Graft. Vizient's clients include academic medical centers, community hospitals, and integrated health delivery networks serving over 65% of the nation's acute care providers.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2020-11-05
Description

Surgi-One is the Canadian distributor for i-FACTOR products including i-FACTOR+ Matrix and other Cerapedics bone graft products in Canada.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2017-10-25
Description

Global life sciences company partnership mentioned in context of Cerapedics 'embarking on the next phase of commercializing novel osteobiologic products.'

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2016-11-30
Description

Cerapedics was awarded a group purchasing agreement with Premier Inc. for Breakthrough Technology: Bone Tissue Synthetic Implantable Products. The agreement allows Premier members to access special pricing and terms pre-negotiated for i-FACTOR Peptide Enhanced Bone Graft. Premier unites approximately 3,750 U.S. hospitals and 130,000 other provider organizations.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global spine market leader with Infuse Bone Graft (rhBMP-2) and broader biologics portfolio including cellular bone matrices. Directly competes with Cerapedics in spine fusion bone grafts while serving as a broad incumbent across all spine surgery categories.

TypeBroad incumbent
Description

Major orthopedic and spine device manufacturer offering OP-1 (BMP-7) bone graft and broader orthobiologics portfolio. Competes with Cerapedics in spine fusion while also serving trauma, joint reconstruction, and other orthopedic segments.

TypeBroad incumbent
Description

Spine and orthobiologics division of J&J offering synthetic bone graft substitutes and demineralized bone matrix products. Competes with Cerapedics in cervical and lumbar fusion bone graft market through established hospital contracts.

TypeDirect peer
Description

Spine-focused medical device company offering bone graft substitutes and orthobiologics alongside its spinal hardware portfolio. Direct competitor to Cerapedics in cervical and lumbar fusion bone graft market with similar target surgeon customers.

TypeDirect peer
Description

Spine and orthopedics company offering bone graft substitutes and biologics including Trinity ELITE and fiberFUSE Strip. Competes directly with Cerapedics in spine fusion orthobiologics with overlapping surgeon customer base.

TypeDirect peer
Description

Pure-play spine company offering OsteoStrand DBM, OsteoSurge DBM putty, and Accell bone matrix products. Direct competitor to Cerapedics in spine fusion biologics with similar commercial model targeting spine surgeons.

TypeDirect peer
Description

Orthobiologics company offering bone graft substitutes including SIGNAFUSE and OSTEOAMP. Direct competitor to Cerapedics in spine and orthopedic bone graft markets with established commercial channels.

TypeDirect peer
Description

Spine and orthopedic-focused orthobiologics company offering bone graft substitutes including OsteoVive Plus, 3Demin, and other DBM/synthetic products. Direct competitor to Cerapedics in spine fusion biologics market with comparable customer base.

TypeEmerging player
Description

Orthobiologics company offering Influx bone graft substitute and other cell-based and synthetic bone graft products. Niche competitor in spine and orthopedic fusion markets with partial overlap with Cerapedics' P-15 technology approach.

TypeEmerging player
Description

Non-profit tissue banking organization offering allograft bone graft products including VertiGraft and cellular bone matrices. Competes with Cerapedics in spine fusion through allograft-based alternatives, especially for surgeons preferring biological options.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers4 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles7 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds13 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors10 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Cerapedics

Spinal Bone Graft Substitutes / Orthobiologicscerapedics.com

Cerapedics is a Westminster, Colorado-based medical device company that develops and commercializes FDA PMA-approved P-15 peptide-enhanced bone graft products (i-FACTOR and PearlMatrix) for cervical and lumbar spinal fusion, sold to spine surgeons and hospitals through direct sales and GPO agreements with Premier Inc. and Vizient.

What Cerapedics does

Cerapedics is a privately-held commercial-stage medical device company headquartered in Westminster, Colorado, that develops and commercializes proprietary osteobiologic products for spinal fusion surgery. The company's core technology is the P-15 Osteogenic Cell Binding Peptide, a synthetic 15-amino-acid sequence derived from Type-1 collagen that is bound onto different osteoconductive scaffolds to accelerate bone formation through an attract-attach-activate mechanism. This technology is the basis for two FDA Premarket-Approved Class III drug-device combination products: i-FACTOR, approved in November 2015 for single-level anterior cervical discectomy and fusion (ACDF) and commercially launched in the U.S. in 2016, and PearlMatrix, approved in June 2025 for single-level transforaminal lumbar interbody fusion (TLIF) with expanded indications covering ALIF, PLIF, OLIF, and LLIF approved in January 2026. PearlMatrix is positioned as the first and only bone growth accelerator proven to accelerate lumbar fusion, backed by Level 1 clinical evidence from the ASPIRE IDE study (293 patients across 33 U.S. centers) and six-year i-FACTOR follow-up data showing 98.6% fusion rates.

Cerapedics generates revenue through direct hardware sales of bone graft products to hospitals and surgical centers, sold via a combination of direct sales representatives, local distribution partners, and group purchasing organization agreements with Premier Inc. and Vizient (the latter covering over 65% of U.S. acute care providers). International sales of i-FACTOR products are conducted through distributors, including Surgi-One in Canada, alongside CE Mark and TGA-listed products. The company serves spine surgeons and neurosurgeons performing cervical and lumbar fusion procedures, with named customers including Cleveland Clinic, Washington University School of Medicine, AdventHealth Avista, and Austin Brain and Spine. Pricing is not publicly disclosed, but products target the U.S. spinal bone graft substitution market, where approximately 465,000 fusion cases were performed in 2023.

The company employs approximately 250 people worldwide, has raised over $180 million cumulatively since 2007 across equity and debt rounds, and is led by Chairman and CEO Valeska Schroeder (appointed November 2022). KCK Group has been the lead institutional investor since a $22 million round in 2018, and the company is controlled by KCK Group as parent investor. The company has been recognized with industry awards including the 2018 MedTech Breakthrough Award for Best New Surgical Technology and Denver Post Top Workplaces in 2024 and 2026.

Cerapedics firmographics

Firmographics
Name
Cerapedics
Legal name
Cerapedics Inc.
Website
https://cerapedics.com
Company type
Private
Founded year
2015
Operating status
Operating
Headcount range
101–250 employees
Short description
Cerapedics is a Westminster, Colorado-based medical device company that develops and commercializes FDA PMA-approved P-15 peptide-enhanced bone graft products (i-FACTOR and PearlMatrix) for cervical and lumbar spinal fusion, sold to spine surgeons and hospitals through direct sales and GPO agreements with Premier Inc. and Vizient.
Ownership category
akta.pro rank

Cerapedics industry classification

Industry
Product category
Spinal Bone Graft Substitutes / Orthobiologics
NAICS
Surgical Appliance and Supplies Manufacturing (339113), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Orthopedic, Prosthetic & Surgical Appliances & Supplies (3842), Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Bone Graft Substitutes & Orthobiologics (Synthetic/Allograft/DBM) (HLAHAEAG)
akta.pro secondary industries
Tissue-Engineered Constructs & Scaffolds (natural/synthetic biomaterials) (HLAAAGAB), Spine Implants & Motion Preservation (Fusion/Disc/Interspinous) (HLAHAEAC)

Keywords

  • Bone graft substitutes
  • Spinal fusion devices
  • Osteobiologic products
  • Peptide enhanced bone graft
  • Spine surgery implants

Where Cerapedics is headquartered

Location

Headquarters

HQ city
Westminster
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Cerapedics business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Operations, Personnel, Marketing or Sales, Supply Chain

Revenue model

  1. i-FACTOR Bone Graft: FDA PMA-approved Class III drug-device combination product for single-level anterior cervical discectomy and fusion (ACDF). Commercialized since 2015/2016 in the U.S. market.
  2. PearlMatrix Bone Graft: FDA PMA-approved Class III drug-device combination product for single-level transforaminal lumbar interbody fusion (TLIF). Approved June 2025 and now approved for expanded indications including ALIF, PLIF, OLIF, and LLIF approaches.
  3. International Products: i-FACTOR products available internationally including i-FACTOR Putty and i-FACTOR Flex FR distributed through international markets. Products also available in Canada through distributor Surgi-One.

Go-to-market motion2 records

Distribution channels5 records

Marketing channels7 records

Cerapedics product offering

Product offering

Core offering

Cerapedics develops, manufactures, and commercializes novel osteobiologic bone graft products based on its proprietary P-15 Osteogenic Cell Binding Peptide technology. The company sells FDA PMA-approved Class III drug-device combination products, including i-FACTOR for cervical spine fusion (ACDF) and PearlMatrix for lumbar spine fusion (TLIF, ALIF, PLIF, OLIF, LLIF), targeting spine surgeons and healthcare facilities worldwide.

Differentiator

Problem solved

Functional benefit

Brands

  • PearlMatrix: P-15 Peptide Enhanced Bone Graft - FDA-approved Class III drug-device combination product for lumbar spine fusion (TLIF procedures). The first and only bone growth accelerator proven to accelerate lumbar fusion.
  • i-FACTOR

Products and services

  • i-FACTOR P-15 Peptide Enhanced Bone Graft FDA PMA-approved Class III drug-device combination bone graft using P-15 Osteogenic Cell Binding Peptide technology for single-level anterior cervical discectomy and fusion (ACDF) procedures in patients with degenerative cervical disc disease. Has been used by surgeons since 2015/2016, with six-year IDE follow-up data showing 98.6% fusion rate. Targeted at spine surgeons seeking a clinically proven, cost-effective alternative to autograft for cervical fusion.
  • PearlMatrix P-15 Peptide Enhanced Bone Graft FDA PMA-approved Class III drug-device combination bone graft using P-15 Osteogenic Cell Binding Peptide technology bound onto a flexible collagen matrix carrier. Indicated for single-level TLIF and now expanded for all major lumbar interbody surgical approaches (ALIF, PLIF, OLIF, LLIF). The first and only bone growth accelerator demonstrated to accelerate lumbar fusion in Level 1 IDE clinical data, with statistically superior time to fusion versus local autograft. Targeted at spine surgeons treating degenerative disc disease.
  • i-FACTOR Flex FR Bone graft substitute utilizing P-15 Osteogenic Cell Binding Peptide technology with purified silk fibers as an inert carrier, providing enhanced cohesion, mechanical properties, and handling characteristics. Sterilized after packaging (terminally sterilized), stored at room temperature, with three-year shelf life, ready to use with no mixing or preparation. Distributed internationally.
  • i-FACTOR Putty Bone graft substitute utilizing P-15 Osteogenic Cell Binding Peptide technology. Terminally sterilized after packaging, stored at room temperature, three-year shelf life, ready to use with no mixing or preparation required. Distributed internationally.
  • i-FACTOR+ Matrix Next-generation P-15 Peptide Enhanced Bone Graft product approved by Health Canada, distributed in Canada through partner Surgi-One.

Quantifiable outcome

  • More than twice as many patients fused at six months vs. local autograft in TLIF procedures
  • +4 more outcomes

Companies that use Cerapedics

Customer profile

Named customers4 records

Segments3 records

Ideal customer profiles1 record

Cerapedics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Cerapedics partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and minor.

  • VizientcoreChannel Partner/ Reseller/ Distributor · 24 April 2026Cerapedics announced a supplier agreement with Vizient, the nation's largest provider-driven healthcare performance improvement company, to distribute PearlMatrix P-15 Peptide Enhanced Bone Graft. Vizient's clients include academic medical centers, community hospitals, and integrated health delivery networks serving over 65% of the nation's acute care providers.
  • Surgi-OnecoreChannel Partner/ Reseller/ Distributor · 5 November 2020Surgi-One is the Canadian distributor for i-FACTOR products including i-FACTOR+ Matrix and other Cerapedics bone graft products in Canada.
  • DSM MedicalminorStrategic or Co-development Partner · 25 October 2017Global life sciences company partnership mentioned in context of Cerapedics 'embarking on the next phase of commercializing novel osteobiologic products.'
  • Premier Inc.coreChannel Partner/ Reseller/ Distributor · 30 November 2016Cerapedics was awarded a group purchasing agreement with Premier Inc. for Breakthrough Technology: Bone Tissue Synthetic Implantable Products. The agreement allows Premier members to access special pricing and terms pre-negotiated for i-FACTOR Peptide Enhanced Bone Graft. Premier unites approximately 3,750 U.S. hospitals and 130,000 other provider organizations.

Scale indicators10 records

Recent moves8 records

Expansion highlights6 records

Cerapedics competitors and assessment

Company assessment

Broad incumbents

  • Medtronic: Global spine market leader with Infuse Bone Graft (rhBMP-2) and broader biologics portfolio including cellular bone matrices. Directly competes with Cerapedics in spine fusion bone grafts while serving as a broad incumbent across all spine surgery categories.
  • Stryker: Major orthopedic and spine device manufacturer offering OP-1 (BMP-7) bone graft and broader orthobiologics portfolio. Competes with Cerapedics in spine fusion while also serving trauma, joint reconstruction, and other orthopedic segments.
  • DePuy Synthes (Johnson & Johnson): Spine and orthobiologics division of J&J offering synthetic bone graft substitutes and demineralized bone matrix products. Competes with Cerapedics in cervical and lumbar fusion bone graft market through established hospital contracts.

Direct peers

  • NuVasive: Spine-focused medical device company offering bone graft substitutes and orthobiologics alongside its spinal hardware portfolio. Direct competitor to Cerapedics in cervical and lumbar fusion bone graft market with similar target surgeon customers.
  • Orthofix Medical: Spine and orthopedics company offering bone graft substitutes and biologics including Trinity ELITE and fiberFUSE Strip. Competes directly with Cerapedics in spine fusion orthobiologics with overlapping surgeon customer base.
  • SeaSpine: Pure-play spine company offering OsteoStrand DBM, OsteoSurge DBM putty, and Accell bone matrix products. Direct competitor to Cerapedics in spine fusion biologics with similar commercial model targeting spine surgeons.
  • Bioventus: Orthobiologics company offering bone graft substitutes including SIGNAFUSE and OSTEOAMP. Direct competitor to Cerapedics in spine and orthopedic bone graft markets with established commercial channels.
  • Xtant Medical: Spine and orthopedic-focused orthobiologics company offering bone graft substitutes including OsteoVive Plus, 3Demin, and other DBM/synthetic products. Direct competitor to Cerapedics in spine fusion biologics market with comparable customer base.

Emerging players

  • Isto Biologics: Orthobiologics company offering Influx bone graft substitute and other cell-based and synthetic bone graft products. Niche competitor in spine and orthopedic fusion markets with partial overlap with Cerapedics' P-15 technology approach.
  • LifeNet Health: Non-profit tissue banking organization offering allograft bone graft products including VertiGraft and cellular bone matrices. Competes with Cerapedics in spine fusion through allograft-based alternatives, especially for surgeons preferring biological options.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Cerapedics social profiles

Digital presence

Cerapedics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Cerapedics leadership team

Management profile

Number of profiles

Profiles7 records

Cerapedics funding detail

Funding detail

Funding overview

Funding rounds13 records

Investors10 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Cerapedics M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Cerapedics

What does Cerapedics do?

Cerapedics develops, manufactures, and commercializes novel osteobiologic bone graft products based on its proprietary P-15 Osteogenic Cell Binding Peptide technology. The company sells FDA PMA-approved Class III drug-device combination products, including i-FACTOR for cervical spine fusion (ACDF) and PearlMatrix for lumbar spine fusion (TLIF, ALIF, PLIF, OLIF, LLIF), targeting spine surgeons and healthcare facilities worldwide.

Is Cerapedics a public or private company?

Cerapedics is a private company. It is classified as private equity controlled and is currently operating.

When was Cerapedics founded?

Cerapedics was founded in 2015. It employs 101 to 250 people.

Where is Cerapedics based?

Cerapedics is headquartered in Westminster, United States, in the North America region.

How does Cerapedics make money?

Three revenue lines are on record. i-FACTOR Bone Graft is the primary driver. The others are pearlMatrix Bone Graft and international Products.

Who are Cerapedics's main competitors?

Broad incumbents on record are Medtronic, Stryker and DePuy Synthes (Johnson & Johnson). Direct peers are NuVasive, Orthofix Medical, SeaSpine, Bioventus and Xtant Medical. Emerging players are Isto Biologics and LifeNet Health.

Does Cerapedics have an API?

No public API is recorded for Cerapedics.

What industry is Cerapedics in?

Cerapedics's product category is Spinal Bone Graft Substitutes / Orthobiologics. Its primary akta.pro industry code is HLAHAEAG, Bone Graft Substitutes & Orthobiologics (Synthetic/Allograft/DBM), with a secondary code of HLAAAGAB, Tissue-Engineered Constructs & Scaffolds (natural/synthetic biomaterials). Its NAICS code is 339113 and its SIC code is 3842.

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Live signals
PR NewswireCerapedics Announces Supplier Agreement with Vizient for PearlMatrix® P-15 Peptide Enhanced Bone GraftCerapedics Inc. announced a supplier agreement with Vizient, the nation's largest provider-driven healthcare performance improvement company, to distribute PearlMatrix® P-15 Peptide Enhanced Bone Graft, an FDA-approved Class III drug-device combination product for adult patients with degenerative disc disease in the lumbar spine. PearlMatrix is the first and only bone growth accelerator demonstrated to achieve statistically superior fusion speed compared to local autograft, with data from the ASPIRE TLIF IDE study showing more than twice as many patients fused at six months. The agreement expands access to Cerapedics' spinal fusion portfolio for Vizient's clients, which include academic medical centers, community hospitals, and integrated health delivery networks serving over 65% of the nation's acute care providers.PR NewswireCerapedics' PearlMatrix P-15 Peptide Enhanced Bone Graft, The First and Only Proven Bone Growth Accelerator, Now Approved for Expanded Indications for UseCerapedics Inc. announced FDA approval to expand the indications for use and labeling of PearlMatrix P-15 Peptide Enhanced Bone Graft, making it the first and only Class III drug-device spinal bone graft approved for all major lumbar interbody surgical approaches, including ALIF, PLIF, OLIF, and LLIF in addition to the original TLIF approval. The expanded approval also includes use with titanium alloy and PEEK/titanium interbody fusion cages. The supplemental application was approved within three months of submission, building on the initial FDA premarket approval in June 2025 supported by data from the ASPIRE clinical trial.BioSpaceCerapedics Announces Publication in Spine of 24-Month ASPIRE Study Results of PearlMatrix™ P-15 Peptide Enhanced Bone GraftCerapedics Inc. announced publication of 24-month results from the ASPIRE pivotal IDE study in the Spine journal, demonstrating that PearlMatrix P-15 Peptide Enhanced Bone Graft achieved statistically superior clinical success and faster time-to-fusion compared to local autograft in single-level TLIF surgery for adult patients with degenerative disc disease. The prospective, multicenter, randomized controlled study enrolled 293 patients across 33 U.S. centers, with approximately 60 percent classified as high-risk for non-union due to conditions such as type 2 diabetes, obesity, or nicotine use. At 6 months, PearlMatrix showed more than twice as many patients fused compared to local autograft, with higher fusion rates continuing through 24 months.PR NewswireCerapedics Announces Publication in Spine of 24-Month ASPIRE Study Results of PearlMatrix™ P-15 Peptide Enhanced Bone GraftCerapedics Inc. announced the publication of 24-month results from the ASPIRE pivotal IDE study of PearlMatrix P-15 Peptide Enhanced Bone Graft in the Spine journal. The randomized controlled study of 293 patients across 33 U.S. centers demonstrated that PearlMatrix achieved statistically superior clinical success and faster time-to-fusion compared to local autograft in single-level transforaminal lumbar interbody fusion surgery for adult patients with degenerative disc disease. At 6 months, more than twice as many PearlMatrix patients had fused compared to autograft patients, with approximately 60 percent of enrolled patients being high-risk for non-union.NewswireCerapedics Announces Publication in Spine of 24-Month ASPIRE Study Results of PearlMatrix™ P-15 Peptide Enhanced Bone GraftCerapedics Inc. announced the publication of 24-month ASPIRE pivotal U.S. IDE study results in the Spine journal, demonstrating that PearlMatrix P-15 Peptide Enhanced Bone Graft achieved statistically superior clinical success and faster time-to-fusion compared to local autograft in single-level transforaminal lumbar interbody fusion surgery. The study enrolled 293 patients across 33 U.S. centers, with approximately 60% being high-risk patients, and found more than twice as many PearlMatrix patients fused at 6 months compared to autograft. The CEO stated the results position PearlMatrix as the first and only drug-device spinal bone graft product proven to accelerate lumbar fusion in degenerative disc disease patients.GlobeNewswire$10.75+ Bn Spinal Fusion Devices Market Insights, Competitive Landscape, and Forecasts, 2032 - Rising Incidences, Trauma from Road Accidents, and an Increase in Chronic PainResearchAndMarkets.com published a market report on the spinal fusion devices industry, valued at USD 7.13 billion in 2024 and projected to reach USD 10.76 billion by 2032, growing at a CAGR of 5.31%. The market growth is driven by rising incidences of spinal disorders, trauma from road accidents, and chronic lower back pain cases projected to increase globally from 619 million in 2023 to 843 million by 2050. Key players including Zimmer Biomet, Stryker, Medtronic, and Orthofix Medical are actively engaging in product launches and FDA approvals, such as Carlsmed Inc.'s aprevo Cervical ACDF Interbody System cleared in December 2024 and Cerapedics' PearlMatrixT bone graft approved in June 2025.PR NewswireCerapedics Announces FDA Approval of PearlMatrix™ P-15 Peptide Enhanced Bone Graft, The First and Only Proven Bone Growth Accelerator for Lumbar FusionCerapedics Inc. announced FDA premarket approval (PMA) for PearlMatrix™ P-15 Peptide Enhanced Bone Graft, a Class III drug-device combination product for single-level TLIF surgery in adult patients with degenerative disc disease. The ASPIRE pivotal study demonstrated statistically superior fusion speed with more than twice as many patients fused at six months versus local autograft, including approximately 60% high-risk patients. PearlMatrix is the first and only bone growth accelerator proven to accelerate lumbar fusion, making it the second PMA-approved spinal bone graft in Cerapedics' portfolio alongside i-FACTOR, with approximately 465,000 spinal fusion cases using bone graft performed in the US in 2023.Ortho Spine NewsCerapedics’ i-FACTOR P-15 Peptide Enhanced Bone Graft, a Trusted Choice in Bone Graft Solutions, Now Approved for Expanded Indications for Use – Ortho Spine NewsCerapedics Inc. announced that the U.S. Food and Drug Administration (FDA) approved an expansion of indications for its i-FACTOR P-15 Peptide Enhanced Bone Graft, allowing its use with various interbody devices in cervical spine surgeries. This approval enables the product to be used in conjunction with PEEK or titanium cages, addressing a significant portion of the estimated 465,000 annual spinal fusion cases in the United States.PR NewswireCerapedics Reinforces Commitment to Level 1 Evidence with Long-Term Results from Six-Year Pivotal IDE Cervical Study Demonstrating 98.6% Spine Fusion Rates in Patients Treated With i-FACTOR®Cerapedics Inc. announced six-year follow-up data from its pivotal IDE study of i-FACTOR Peptide-Enhanced Bone Graft, showing spine fusion rates of 98.6% in single-level Anterior Cervical Discectomy and Fusion procedures, compared to 97.3% for local autograft control. The study, published in Neurosurgery, followed 220 of the original 319 patients across 17 sites and met all four FDA-mandated non-inferiority success criteria at 12, 24, and 72-month endpoints. The company noted the data provides Level 1 clinical evidence for insurance payers making coverage decisions and is currently conducting a second randomized controlled trial for transforaminal lumbar interbody fusion indication.American City Business JournalsColorado's Cerapedics grows local HQ, plans to hire 60Colorado-based Cerapedics is expanding its local headquarters and plans to hire 60 employees. The additional space brings the company's total footprint to approximately 60,000 square feet, supporting its bone graft product line.