FDA applicant
Pfizer Hospital Products Group, Inc.
FDA records 8 decisions for Pfizer Hospital Products Group, Inc. (Rutherford, NJ) from 1991 to 1994: 8 510(k) clearances. Most are in product codes JWH (Prosthesis, Knee, Patellofemorotibial…) and GAM (Suture, Absorbable, Synthetic, Polyglycolic Acid). 8 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Pfizer Hospital Products Group, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Pfizer Hospital Products Group, Inc. since 2007.
Recalls per year
3in 2023
Class I Class II/III not classified
Planning a device like Pfizer Hospital Products Group, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Pfizer”
FDA records each applicant name separately; these may or may not be the same firm.