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Aspire Bariatrics

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uuid0003574

Namestring
Aspire Bariatrics
Legal namestring
Aspire Bariatrics, Inc.
Company typeenum
Private
Founded yearint
2004
Descriptiontext

Aspire Bariatrics, Inc. was a privately held U.S. medical device company headquartered in King of Prussia, Pennsylvania, founded in 2004 by Moshe Shike, Stephen Solomon, and Samuel Klein. The company developed and commercialized the AspireAssist, a minimally invasive, reversible weight loss device that received FDA premarket approval (PMA) in June 2016. The technology used a surgically placed tube (A-Tube) connected to an external drainage system, enabling patients to aspirate a portion of stomach contents approximately 20-30 minutes after meals as an adjunct to lifestyle and dietary counseling. The mechanism was positioned as an alternative to traditional bariatric surgery for obese patients who sought a non-surgical or reversible intervention.

The AspireAssist was the first FDA-approved device for weight loss via mechanical aspiration, and the company emphasized its safety and effectiveness profile remained consistent with the original PMA throughout the product's commercial life. Distribution was conducted exclusively through physicians and bariatric surgeons, with supplies distributed in interstate commerce subject to the company's PMA. The company employed between 11 and 50 people, led by CEO Kathy Crothall and EVP Sales & Marketing Audrey Finkelstein, with additional leadership in health policy/reimbursement (Toni Harp Bala) and sales (Paul Gallo).

Aspire Bariatrics raised approximately $25.2M across four disclosed funding rounds between 2014 and 2017, with investors including growX ventures, Hercules Capital, and Reservoir Investment Managers. Despite regulatory approval and a differentiated product concept, the company wound down all operations and withdrew the AspireAssist from the market effective April 8, 2022, citing the financial impact of the COVID-19 pandemic. The closure was explicitly attributed to economic factors rather than safety or effectiveness concerns, and the company is no longer operational.

Short descriptiontext

Aspire Bariatrics was a U.S. medical device company that developed the AspireAssist, an FDA-approved (June 2016) aspiration-based weight loss device for obese patients seeking a reversible, minimally invasive alternative to bariatric surgery. The company ceased operations effective April 8, 2022, citing COVID-19 financial impact.

Operating statusenum
Closed
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersKing Of Prussia, United States
HQ citystring
King Of Prussia
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Keyword5 values
bariatric medical devices, weight loss devices, minimally invasive surgery, obesity treatment devices, gastric aspiration systems
Industry1 code
1Obesity Medicine & Weight Management
CodeHLAKADALPrimaryYes
SIC code1 code
  • Orthopedic, Prosthetic & Surgical Appliances & Supplies3842
Product category
Bariatric Medical Devices
Cost components5 values
Operations, Technology or R&D, Personnel, Marketing or Sales, Supply Chain
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1AspireAssist
Description

FDA-approved weight loss device for bariatric patients.

aspirebariatrics.com
Core offering1 text field

Aspire Bariatrics developed, manufactured, and marketed the AspireAssist, a minimally invasive, reversible weight loss medical device that used an externally accessible tube to allow patients to aspirate (drain) a portion of stomach contents after meals. The product received FDA premarket approval in June 2016 and was used in conjunction with lifestyle counseling as a bariatric weight management intervention. The company ceased operations and withdrew the product from the market effective April 8, 2022.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Aspire Bariatrics offered a single core product—the AspireAssist weight management device—supported by the A-Tube component. The company wound down all operations and withdrew the AspireAssist from the market effective April 8, 2022, due to COVID-19 financial impact. The company is no longer operational.

Product and service1 record
1AspireAssist
Categorycore product
Description

FDA-approved (PMA, June 2016) weight loss medical device that uses a tube-based aspiration system to mechanically remove stomach contents after meals, supporting weight management in conjunction with lifestyle and dietary counseling. Withdrawn from the market effective April 8, 2022.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Peers10 records
TypeDirect peer
Description

Developer of the Allurion Balloon, a swallowable, non-surgical intragastric balloon for weight loss. Most direct comparable to AspireAssist as a minimally invasive, device-based obesity intervention targeting patients seeking alternatives to bariatric surgery.

TypeBroad incumbent
Description

Maker of the ORBERA intragastric balloon and OverStitch endoscopic suturing system — overlapping minimally invasive and endoscopic obesity device portfolio. Now part of Boston Scientific, providing broader commercial reach.

TypeDirect peer
Description

Developed the ReShape intragastric balloon and Lap-Band adjustable gastric banding system — directly comparable bariatric devices targeting the same obese-patient segment via minimally invasive mechanisms.

TypeDirect peer
Description

Maker of the Obalon swallowable gas-filled intragastric balloon system for weight loss. Closely analogous minimally invasive, device-based obesity platform and notably also wound down U.S. operations, making it a strong outcome-comparable peer.

TypeEmerging player
Description

Developer of the Spatz3 adjustable intragastric balloon, a niche minimally invasive obesity device. Comparable mechanism of action (endoscopic gastric intervention) and similar patient population, though at smaller commercial scale.

TypeDirect peer
Description

Developed EndoBarrier, an endoscopically delivered duodenal-jejunal bypass liner for metabolic disease and obesity. Highly comparable minimally invasive metabolic device company; similarly faced commercial and regulatory headwinds.

TypeBroad incumbent
Description

Major surgical bariatric franchise through Ethicon Endo-Surgery, including stapling and energy devices used in bariatric surgery. Broad incumbent in the same surgical bariatric space, though not focused on aspiration-based devices.

TypeBroad incumbent
Description

Global medtech incumbent with significant metabolic and bariatric surgery exposure, including surgical stapling and hernia products used in obesity procedures. Competes broadly for the same hospital bariatric procedure volume.

TypeBroad incumbent
Description

Maker of Wegovy (semaglutide) and Saxenda (liraglutide), the dominant GLP-1 obesity pharmacotherapies. Not a device competitor but the defining alternative treatment paradigm competing for the same obese-patient demand pool.

TypeBroad incumbent
Description

Maker of Zepbound (tirzepatide) and Mounjaro, the leading next-generation GLP-1/GIP obesity therapies. Sets the standard-of-care benchmark against which any re-launched AspireAssist would need to position.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat2 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights5 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment1 record

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

Feature1 record

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 rounds4 records

Each record includes

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

Investors3 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 →

Aspire Bariatrics

Bariatric Medical Devicesaspirebariatrics.com

Aspire Bariatrics was a U.S. medical device company that developed the AspireAssist, an FDA-approved (June 2016) aspiration-based weight loss device for obese patients seeking a reversible, minimally invasive alternative to bariatric surgery. The company ceased operations effective April 8, 2022, citing COVID-19 financial impact.

What Aspire Bariatrics does

Aspire Bariatrics, Inc. was a privately held U.S. medical device company headquartered in King of Prussia, Pennsylvania, founded in 2004 by Moshe Shike, Stephen Solomon, and Samuel Klein. The company developed and commercialized the AspireAssist, a minimally invasive, reversible weight loss device that received FDA premarket approval (PMA) in June 2016. The technology used a surgically placed tube (A-Tube) connected to an external drainage system, enabling patients to aspirate a portion of stomach contents approximately 20-30 minutes after meals as an adjunct to lifestyle and dietary counseling. The mechanism was positioned as an alternative to traditional bariatric surgery for obese patients who sought a non-surgical or reversible intervention.

The AspireAssist was the first FDA-approved device for weight loss via mechanical aspiration, and the company emphasized its safety and effectiveness profile remained consistent with the original PMA throughout the product's commercial life. Distribution was conducted exclusively through physicians and bariatric surgeons, with supplies distributed in interstate commerce subject to the company's PMA. The company employed between 11 and 50 people, led by CEO Kathy Crothall and EVP Sales & Marketing Audrey Finkelstein, with additional leadership in health policy/reimbursement (Toni Harp Bala) and sales (Paul Gallo).

Aspire Bariatrics raised approximately $25.2M across four disclosed funding rounds between 2014 and 2017, with investors including growX ventures, Hercules Capital, and Reservoir Investment Managers. Despite regulatory approval and a differentiated product concept, the company wound down all operations and withdrew the AspireAssist from the market effective April 8, 2022, citing the financial impact of the COVID-19 pandemic. The closure was explicitly attributed to economic factors rather than safety or effectiveness concerns, and the company is no longer operational.

Aspire Bariatrics firmographics

Firmographics
Name
Aspire Bariatrics
Legal name
Aspire Bariatrics, Inc.
Website
https://aspirebariatrics.com
Company type
Private
Founded year
2004
Operating status
Closed
Headcount range
11–50 employees
Short description
Aspire Bariatrics was a U.S. medical device company that developed the AspireAssist, an FDA-approved (June 2016) aspiration-based weight loss device for obese patients seeking a reversible, minimally invasive alternative to bariatric surgery. The company ceased operations effective April 8, 2022, citing COVID-19 financial impact.
Ownership category
akta.pro rank

Aspire Bariatrics industry classification

Industry
Product category
Bariatric Medical Devices
SIC
Orthopedic, Prosthetic & Surgical Appliances & Supplies (3842)
akta.pro primary industry
Obesity Medicine & Weight Management (HLAKADAL)

Keywords

  • Bariatric medical devices
  • Weight loss devices
  • Minimally invasive surgery
  • Obesity treatment devices
  • Gastric aspiration systems

Where Aspire Bariatrics is headquartered

Location

Headquarters

HQ city
King Of Prussia
HQ country
United States
HQ region
North America

Markets served

Aspire Bariatrics business model

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

Aspire Bariatrics product offering

Product offering

Core offering

Aspire Bariatrics developed, manufactured, and marketed the AspireAssist, a minimally invasive, reversible weight loss medical device that used an externally accessible tube to allow patients to aspirate (drain) a portion of stomach contents after meals. The product received FDA premarket approval in June 2016 and was used in conjunction with lifestyle counseling as a bariatric weight management intervention. The company ceased operations and withdrew the product from the market effective April 8, 2022.

Product overview

Aspire Bariatrics offered a single core product—the AspireAssist weight management device—supported by the A-Tube component. The company wound down all operations and withdrew the AspireAssist from the market effective April 8, 2022, due to COVID-19 financial impact. The company is no longer operational.

Differentiator

Problem solved

Functional benefit

Brands

  • AspireAssist: FDA-approved weight loss device for bariatric patients.

Products and services

  • AspireAssist FDA-approved (PMA, June 2016) weight loss medical device that uses a tube-based aspiration system to mechanically remove stomach contents after meals, supporting weight management in conjunction with lifestyle and dietary counseling. Withdrawn from the market effective April 8, 2022.

Companies that use Aspire Bariatrics

Customer profile

Segments1 record

Ideal customer profiles1 record

Aspire Bariatrics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature1 record

Aspire Bariatrics partnerships and signals

Strategic signal

Recent moves7 records

Aspire Bariatrics competitors and assessment

Company assessment

Direct peers

  • Allurion Technologies: Developer of the Allurion Balloon, a swallowable, non-surgical intragastric balloon for weight loss. Most direct comparable to AspireAssist as a minimally invasive, device-based obesity intervention targeting patients seeking alternatives to bariatric surgery.
  • ReShape Lifesciences: Developed the ReShape intragastric balloon and Lap-Band adjustable gastric banding system — directly comparable bariatric devices targeting the same obese-patient segment via minimally invasive mechanisms.
  • Obalon Therapeutics: Maker of the Obalon swallowable gas-filled intragastric balloon system for weight loss. Closely analogous minimally invasive, device-based obesity platform and notably also wound down U.S. operations, making it a strong outcome-comparable peer.
  • GI Dynamics: Developed EndoBarrier, an endoscopically delivered duodenal-jejunal bypass liner for metabolic disease and obesity. Highly comparable minimally invasive metabolic device company; similarly faced commercial and regulatory headwinds.

Broad incumbents

  • Apollo Endosurgery (acquired by Boston Scientific): Maker of the ORBERA intragastric balloon and OverStitch endoscopic suturing system — overlapping minimally invasive and endoscopic obesity device portfolio. Now part of Boston Scientific, providing broader commercial reach.
  • Ethicon (Johnson & Johnson): Major surgical bariatric franchise through Ethicon Endo-Surgery, including stapling and energy devices used in bariatric surgery. Broad incumbent in the same surgical bariatric space, though not focused on aspiration-based devices.
  • Medtronic: Global medtech incumbent with significant metabolic and bariatric surgery exposure, including surgical stapling and hernia products used in obesity procedures. Competes broadly for the same hospital bariatric procedure volume.
  • Novo Nordisk: Maker of Wegovy (semaglutide) and Saxenda (liraglutide), the dominant GLP-1 obesity pharmacotherapies. Not a device competitor but the defining alternative treatment paradigm competing for the same obese-patient demand pool.
  • Eli Lilly: Maker of Zepbound (tirzepatide) and Mounjaro, the leading next-generation GLP-1/GIP obesity therapies. Sets the standard-of-care benchmark against which any re-launched AspireAssist would need to position.

Emerging players

  • Spatz FGIA: Developer of the Spatz3 adjustable intragastric balloon, a niche minimally invasive obesity device. Comparable mechanism of action (endoscopic gastric intervention) and similar patient population, though at smaller commercial scale.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat2 records

Key risks6 records

Key highlights5 records

Customer concentration

Aspire Bariatrics social profiles

Digital presence

Aspire Bariatrics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Aspire Bariatrics leadership team

Management profile

Number of profiles

Profiles7 records

Aspire Bariatrics funding detail

Funding detail

Funding overview

Funding rounds4 records

Investors3 records

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

Aspire Bariatrics 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 Aspire Bariatrics

What does Aspire Bariatrics do?

Aspire Bariatrics developed, manufactured, and marketed the AspireAssist, a minimally invasive, reversible weight loss medical device that used an externally accessible tube to allow patients to aspirate (drain) a portion of stomach contents after meals. The product received FDA premarket approval in June 2016 and was used in conjunction with lifestyle counseling as a bariatric weight management intervention. The company ceased operations and withdrew the product from the market effective April 8, 2022.

Is Aspire Bariatrics a public or private company?

Aspire Bariatrics is a private company. It is classified as venture growth investor backed and is currently closed.

When was Aspire Bariatrics founded?

Aspire Bariatrics was founded in 2004. It employs 11 to 50 people.

Where is Aspire Bariatrics based?

Aspire Bariatrics is headquartered in King Of Prussia, United States, in the North America region.

Who are Aspire Bariatrics's main competitors?

Direct peers on record are Allurion Technologies, ReShape Lifesciences, Obalon Therapeutics and GI Dynamics. Broad incumbents are Apollo Endosurgery (acquired by Boston Scientific), Ethicon (Johnson & Johnson), Medtronic, Novo Nordisk and Eli Lilly. Spatz FGIA is listed as an emerging player.

Does Aspire Bariatrics have an API?

No public API is recorded for Aspire Bariatrics.

What industry is Aspire Bariatrics in?

Aspire Bariatrics's product category is Bariatric Medical Devices. Its primary akta.pro industry code is HLAKADAL, Obesity Medicine & Weight Management. Its SIC code is 3842.

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Live signals
PR NewswireAspireAssist® Pivotal Trial Results Published in the American Journal of GastroenterologyAspire Bariatrics announced the publication of PATHWAY study results in the American Journal of Gastroenterology, a 171-subject multicenter randomized control trial of the AspireAssist endoscopic weight loss device. After 52 weeks of therapy, patients lost 37% of excess weight on average along with clinically significant improvements in HbA1C, triglycerides, and HDL cholesterol, with no adverse eating behaviors reported; the device received FDA premarket approval in June 2016. The CEO highlighted a significant unmet need given that fewer than 1% of eligible Americans with BMI over 35 undergo bariatric surgery, noting the device offers a lower-cost alternative and publication should facilitate insurance coverage.PR NewswireFDA approves AspireAssist obesity deviceThe U.S. Food and Drug Administration approved the AspireAssist obesity treatment device on June 14, 2016, making it available for patients aged 22 and older with a BMI of 35 to 55 who have not achieved weight loss through non-surgical therapy. Clinical trial data showed patients using the device lost an average of 12.1 percent of body weight after one year, compared to 3.6 percent for patients receiving lifestyle therapy alone, with the device removing approximately 30 percent of calories consumed. The AspireAssist is manufactured by Aspire Bariatrics and includes safety features such as an automatic shutoff after 115 use cycles.PR NewswireLa FDA aprueba el dispositivo AspireAssist contra la obesidadThe U.S. Food and Drug Administration (FDA) approved the AspireAssist obesity treatment device on June 14, 2016, which uses a surgically inserted tube to drain approximately 30% of stomach contents after meals. Clinical trial data showed that patients using the device lost an average of 12.1% of their body weight after one year, compared to 3.6% for patients receiving lifestyle therapy alone. The device is manufactured by Aspire Bariatrics, based in King of Prussia, Pennsylvania, and is designed for obese adults aged 22 and older with a BMI between 35 and 55.PR NewswireFDA Approves the AspireAssist®, a Minimally-Invasive Alternative to Weight Loss Surgery for People with Moderate to Severe ObesityThe US Food and Drug Administration has approved the AspireAssist System, a minimally-invasive endoscopic device for weight loss developed by Aspire Bariatrics. The procedure is indicated for adults with moderate to severe obesity who have not succeeded with conservative therapies and offers a reversible alternative to bariatric surgery.FinSMEsAspire Bariatrics Secures $12M Venture Loan Facility with HTGCAspire Bariatrics closed up to $12M in venture debt financing from Hercules Technology Growth Capital. The funds will support its PATHWAY pivotal trial and a PMA filing expected in mid-2015. The device is already approved for commercial sale in Europe.VC News DailyAspire Bariatrics Secures $12M Venture DebtAspire Bariatrics, a medical device company based in King of Prussia, Pennsylvania, has secured up to $12 million in venture debt financing from Hercules Technology Growth Capital. The funding will support the company's PATHWAY pivotal trial and FDA Pre-Market Application filing for the AspireAssist weight loss device, expected in mid-2015, with US market entry anticipated in early 2016. The device, currently completing its multicenter randomized controlled trial at ten leading US hospital institutions, is designed as a reversible, minimally-invasive weight loss solution that does not alter patient anatomy.