FDA applicant

Biocore Medical Technologies, Inc.

Silver Spring, MD4 decisions2001–20020 recalls

FDA records 4 decisions for Biocore Medical Technologies, Inc. (Silver Spring, MD) from 2001 to 2002: 4 510(k) clearances. Most are in product codes MGP (Dressing, Wound And Burn, Occlusive) and KGN (Wound Dressing With Animal-Derived Material (S)). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

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

FDA decisions per year

No FDA decision for Biocore Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Biocore Medical Technologies, 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 “Biocore”

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

Biocore 3

Biocore Medical Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Biocore”