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Data / Medical devices / Pump, Portable, Aspiration (Manual Or Powered) / United States

FDA-registered makers of Pump, Portable, Aspiration (Manual Or Powered) in the United States: 28 establishments

28 establishments in the United States are registered with the FDA to make Pump, Portable, Aspiration (Manual Or Powered) (product code BTA). 21 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

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Device
Pump, Portable, Aspiration (Manual Or Powered)
Product code
BTA
Country
United States

Makers of Pump, Portable, Aspiration (Manual Or Powered) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ohio Medical LLCGurnee, IL, United StatesComplaint file establishment, Manufacturer4April 27, 2010040api.fda.gov
Sscor, Inc.Simi Valley, CA, United StatesManufacturer4May 18, 2004010api.fda.gov
Allied Medical LLCEarth City, MO, United StatesManufacturer, Specification developer2August 21, 1995000api.fda.gov
Karl Storz Endoscopy-America, Inc.Auburn, MA, United StatesContract manufacturer, Repackager or relabeler2August 12, 1998000api.fda.gov
Medgyn Products, Inc.Westmont, IL, United StatesManufacturer, Repackager or relabeler2June 8, 2001000api.fda.gov
Precision Medical, Inc.Northampton, PA, United StatesManufacturer2April 1, 1998010api.fda.gov
Centese, Inc.Omaha, NE, United StatesManufacturer1November 29, 2018000api.fda.gov
DRW MedicalAston, PA, United StatesManufacturer1September 16, 2022000api.fda.gov
Gi SupplyMechanicsburg, PA, United StatesManufacturer1April 19, 2023000api.fda.gov
Haemonetics CorporationBoston, MA, United StatesSpecification developer1October 5, 2005010api.fda.gov
Medco MFG.Spring, TX, United StatesManufacturer1February 12, 1999000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer1May 4, 2021000api.fda.gov
Microsurgical Technology, Inc.Redmond, WA, United StatesComplaint file establishment, Manufacturer, Specification developer1February 17, 2004000api.fda.gov
Penumbra, Inc.Alameda, CA, United StatesManufacturer1August 17, 2005000api.fda.gov
Penumbra Inc.Roseville, CA, United StatesManufacturer1August 17, 2005000api.fda.gov
Penumbra Inc.Salt Lake City, UT, United StatesManufacturer1August 17, 2005000api.fda.gov
Penumbra Inc.Livermore, CA, United StatesManufacturer1August 17, 2005000api.fda.gov
R & D Batteries, Inc.Burnsville, MN, United StatesManufacturer1June 28, 1994000api.fda.gov
Somavac Medical Solutions, Inc.Memphis, TN, United StatesManufacturer1May 31, 2018000api.fda.gov
Wells Johnson Co.Tucson, AZ, United StatesManufacturer1October 20, 1983000api.fda.gov
Zoll Medical CorporationChelmsford, MA, United StatesComplaint file establishment, Manufacturer1April 18, 2017000api.fda.gov
Axcesor LLCMenomonee Falls, WI, United StatesContract manufacturer0000api.fda.gov
Cro, LLCMissoula, MT, United StatesContract manufacturer0000api.fda.gov
Isomedix Operations Inc.San Diego, CA, United StatesManufacturer for export0000api.fda.gov
MicroVention, Inc.Aliso Viejo, CA, United StatesSpecification developer0000api.fda.gov
Sedation Systems LLCTierra Verde, FL, United StatesSpecification developer0000api.fda.gov
Ventec Life Systems, Inc.Woodinville, WA, United StatesManufacturer0000api.fda.gov
Ventec Life Systems, Inc.Bothell, WA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.