FDA applicant

Kinetic Biomedical Services, Inc.

Erie, PA5 decisions1989–19890 recalls

FDA records 5 decisions for Kinetic Biomedical Services, Inc. (Erie, PA) in 1989: 5 510(k) clearances. Most are in product codes FSY (Light, Surgical, Ceiling Mounted) and FSS (Light, Surgical, Floor Standing). 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 Biomedical Services, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kinetic Biomedical Services, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Kinetic”

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

Kinetic Medical Products 63 Kinetic Concepts, Inc. 48 Kinetic Technology, 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 Biomedical Services, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kinetic”