FDA applicant

Biomed Personal Metabolic and Nutritional Testing

Memphis, TN2 decisions2003–20030 recalls

FDA records 2 decisions for Biomed Personal Metabolic and Nutritional Testing (Memphis, TN) in 2003: 2 510(k) clearances. All are in product code JKA (Tubes, Vials, Systems, Serum Separators, Blood…). 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, clinical chemistry panel, where it files most

How often FDA has decided Biomed Personal Metabolic and Nutritional Testing’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biomed Personal Metabolic and Nutritional Testing since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Biomed Personal Metabolic and Nutritional Testing 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 Biomed Devices Corp. 2 The Biomed Group 2 Biomed Laboratories, Inc. 1 Biomed Ent, Inc. 1 Biomed Products 1

Biomed Personal Metabolic and Nutritional Testing

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Biomed”