FDA applicant

Kinetic Medical Products

Erie, PA63 decisions1989–19890 recalls

FDA records 63 decisions for Kinetic Medical Products (Erie, PA) in 1989: 63 510(k) clearances. Most are in product codes HTD (Forceps) and HXD (Clamp). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Kinetic Medical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kinetic Medical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kinetic Medical Products by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Kinetic Medical Products’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) Report

Other applicant names beginning “Kinetic”

FDA records each applicant name separately; these may or may not be the same firm.

Kinetic Concepts, Inc. 48 Kinetic Technology, Inc. 5 Kinetic Biomedical Services, Inc. 5 Kinetic Instruments, Inc. 2 Kinetic Surgical, LLC 2 Kinetic Rehabilitation Instruments, Inc. 1 Kinetic Resources, Inc. 1 Kinetic Innovative Seating System, LLC 1

Kinetic Medical Products

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Kinetic”