FDA applicant

Biomed Devices Corp.

Grand Junction, CO2 decisions1997–19970 recalls

FDA records 2 decisions for Biomed Devices Corp. (Grand Junction, CO) in 1997: 2 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). 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, ophthalmic panel, where it files most

How often FDA has decided Biomed Devices Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biomed Devices Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Biomed”

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

Biomed Diagnostics, Inc. 3 The Biomed Group 2 Biomed Personal Metabolic and Nutritional Testing 2 Biomed Laboratories, Inc. 1 Biomed Ent, Inc. 1 Biomed Products 1

Biomed Devices Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Biomed”