FDA applicant

Devmed Corp.

Palm Beach Gardens, FL3 decisions1993–19970 recalls

FDA records 3 decisions for Devmed Corp. (Palm Beach Gardens, FL) from 1993 to 1997: 3 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and ITX (Transducer, Ultrasonic, Diagnostic). Its devices cite 5 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, gastroenterology and urology panel, where it files most

How often FDA has decided Devmed Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Devmed Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Devmed Corp.’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 “Devmed”

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

Devmed Group, Inc. 2

Devmed Corp.

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 “Devmed”