FDA applicant

Advance Medical Device, Inc.

Camden, NJ5 decisions1990–19970 recalls

FDA records 5 decisions for Advance Medical Device, Inc. (Camden, NJ) from 1990 to 1997: 5 510(k) clearances. Most are in product codes JAF (Monitor, Ultrasonic, Nonfetal) and JOP (Transducer, Ultrasonic). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Advance Medical Device, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Advance Medical Device, 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 “Advance”

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

Advance Medical Designs, Inc. 32 Advance Suture, Inc. 5 Advance Rubber, Inc. 3 Advance Sentry Corporation 1 Advance Tech Intl. 1 Advance Corp. 1

Advance Medical Device, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Advance”