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Pfizer Hospital Products Group, Inc.

United StatesFDA applicant, unverified

Devices
8

What Pfizer Hospital Products Group, Inc. makes

Pfizer Hospital Products Group, Inc. manufactures medical devices including the PLEUR-EVAC PLUS CONTINUOUS REINFUSION & AUTOINFUSION SYSTEM, MEGA PLUS SUPER LAG SCREW, DURACON MODULAR FEMORAL COMPONENT AND FEMORAL SPAC, SCHNEIDER WALLSTENT(R), HOWMEDICA ALUMINA FEMORAL HEAD, DURACON TOTAL KNEE SYSTEM TIBIAL COMPONENTS, BONDEK POLYGLYCOLIC ACID SYNTHETIC ABSORBABLE SUTURE, and PCA TOTAL HIP SYSTEM (CEMENTLESS USE).

The company's portfolio consists of Class II devices listed in the FDA 510(k) registry. Pfizer Hospital Products Group, Inc. is based in the US.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue8

Newest first, rows 1-8 of 8

Frequently asked questions

How many devices does Pfizer Hospital Products Group, Inc. have in the registry?

The registry currently lists 8 devices for Pfizer Hospital Products Group, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Pfizer Hospital Products Group, Inc.'s devices?

Among its 8 most recently registered devices, Pfizer Hospital Products Group, Inc. has devices listed in FDA 510(k) (8 devices).

What risk classes do Pfizer Hospital Products Group, Inc.'s devices fall under?

Among its 8 most recently registered devices, the classes recorded for Pfizer Hospital Products Group, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Pfizer Hospital Products Group, Inc. in the registry?

The most recently registered devices listed for Pfizer Hospital Products Group, Inc. include PLEUR-EVAC PLUS CONTIN. REINFUS. & AUTOINFUS. SYST, MEGA PLUS SUPER LAG SCREW, DURACON MODULAR FEMORAL COMPONENT AND FEMORAL SPAC and SCHNEIDER WALLSTENT(R).

Generated automatically from registry data and not verified by a human reviewer.