FDA applicant

Telcam Medical Devices, Inc.

Walker, MI3 decisions1981–19830 recalls

FDA records 3 decisions for Telcam Medical Devices, Inc. (Walker, MI) from 1981 to 1983: 3 510(k) clearances. Most are in product codes KNX (Collector, Urine, (And Accessories) For…) and EYQ (Garment, Protective, For Incontinence). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Telcam Medical Devices, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Telcam Medical Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Telcam Medical Devices, Inc.

Which product codes does it file in?

What has FDA decided for it lately?