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Data / Medical devices / Implant, Muscle, Pectoralis

Implant, Muscle, Pectoralis (MIC): 3 FDA-registered makers in 1 country

3 establishments in 1 country are registered with the FDA to make Implant, Muscle, Pectoralis (product code MIC, Class 2, 21 CFR 874.3620). 3 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 8 510(k) clearances under this code, the latest on July 3, 2002, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code
MIC
Device class
2
Regulation
874.3620
Medical specialty
Ear, Nose, Throat
Implant
Yes

Makers by country

CountryMakers
United States3

Makers of Implant, Muscle, Pectoralis

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Dsaart, LLCCarson City, NV, United StatesManufacturer1July 3, 2002010api.fda.gov
Hanson Medical, Inc.Paso Robles, CA, United StatesManufacturer1December 24, 1997000api.fda.gov
Implantech Associates, Inc.Ventura, CA, United StatesManufacturer1November 7, 1994000api.fda.gov

Updated July 3, 2002. 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.