FDA applicant

Apex Medical Technologies, Inc.

San Diego, CA8 decisions1987–20120 recalls

FDA records 8 decisions for Apex Medical Technologies, Inc. (San Diego, CA) from 1987 to 2012: 8 510(k) clearances. Most are in product codes HIS (Condom) and KGO (Surgeon'S Gloves). Its devices cite 9 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

FIG. A — Illustration, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

1in 2012

2007high 1 (2012) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Apex 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.

See the 510(k) Report

Other applicant names beginning “Apex”

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

Apex Medical Corp. 36 Apex BioTechnology Corp. 35 Apex Dental Materials, Inc. 15 Apex Surgical, LLC 6 Apex Metal, Inc. 3 Apex Tools & Orthopedics Co. 2 Apex Ent., Inc. 1 Apex Optical Ind. Co. 1 Apex Medical Products, LLC 1 Apex Technologies, Inc. 1 Apex Orthodontics, Inc. 1 Apex Imaging Corp. 1

Apex 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 “Apex”