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Data / Medical devices / United States / Wyeth Pharmaceuticals LLC

Wyeth Pharmaceuticals LLC: FDA-registered device maker in Collegeville, PA, United States, 1 PMA approval

Wyeth Pharmaceuticals LLC is registered with the FDA (registration 1000150646) in Collegeville, PA, United States. It lists 3 device types. The FDA files 1 PMA approval under its listings, the newest dated July 8, 1983. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1000150646
FEI number
3004393730
Address
500 Arcola Road, Collegeville, PA, United States, 19426
Owner or operator
PFIZER INC. (9924008)
Roles
Complaint file establishment
First device listed
December 2, 2008
Registered through
2026
Brand names listed
CARPUJECT HOLDER, GEL-FLOW NT, Gel-Flow Kit 6mL, Genotropin Pen

Devices it lists

DeviceProduct codeClassRoleSource
Adaptor, Holder, SyringeIQG1Complaint file establishmentaccessdata.fda.gov
Agent, Absorbable Hemostatic, Collagen BasedLMF3Complaint file establishmentaccessdata.fda.gov
Injector, PenNSC2Complaint file establishmentaccessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

ApprovedPMA numberDeviceProduct codeSupplementsLatest decisionSource
July 8, 1983N18286GELFOAMLMF37May 16, 2023accessdata.fda.gov

Compare with other makers

Updated May 16, 2023. 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.