FDA applicant

Deep Blue Medical Advances, Inc.

Durham, NC4 decisions2020–20230 recalls

FDA records 4 decisions for Deep Blue Medical Advances, Inc. (Durham, NC) from 2020 to 2023: 4 510(k) clearances. All are in product code FTL (Mesh, Surgical, Polymeric). Since 2016 its 510(k)s took a median of 84 days from receipt to decision, against 84 for FDA’s reviews in the same codes and years. Its devices cite 7 predicates, 6 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

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Deep Blue Medical Advances, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2023

2020high 2 (2023) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Deep Blue Medical Advances, Inc. by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Other applicant names beginning “Deep”

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

Deep Breeze, Ltd. 3 Deep Breathe, Inc. 2 Deep Trading Corp. 1 Deep Reasoning Ai, Inc. 1

Deep Blue Medical Advances, Inc.

Which product codes does it file in?

How long do its 510(k) reviews take?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Deep”