FDA applicant

Derma Media Lab., Inc.

Santa Fe Springs, CA18 decisions1996–19970 recalls

FDA records 18 decisions for Derma Media Lab., Inc. (Santa Fe Springs, CA) from 1996 to 1997: 18 510(k) clearances. Most are in product codes CEO (Phosphomolybdate (Colorimetric), Inorganic…) and CDQ (Urease And Glutamic Dehydrogenase, Urea Nitrogen). 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 Derma Media Lab., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Derma Media Lab., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Derma Media Lab., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Derma”

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

Derma Sciences, Inc. 22 Derma-Lase Co. 5 Derma Sciences Canada, Inc. 3 Derma-Lock Medical Corp. 2 Derma-Safe Co. 2 Derma Care Plus Products, LLC 2

Derma Media Lab., Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Derma”