510(k) Report

FDA applicant

Voss Medical Products

San Antonio, TX5 decisions1989–19930 recalls

FDA records 5 decisions for Voss Medical Products (San Antonio, TX) from 1989 to 1993: 5 510(k) clearances. Most are in product codes KIL (Positioner, Socket) and FQO (Table, Operating-Room, Ac-Powered). 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 Voss Medical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Voss Medical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Voss”

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