FDA applicant

Hill-Med, Inc.

Miami, FL10 decisions1993–20000 recalls

FDA records 10 decisions for Hill-Med, Inc. (Miami, FL) from 1993 to 2000: 10 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and HEX (Colposcope (And Colpomicroscope)). Its devices cite 1 predicate, 1 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 Hill-Med, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hill-Med, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Hill-Med, 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 “Hill-Med”

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

Hill-Rom, Inc. 37 Hill Laboratories Co. 17 Hill-Rom Air-Shields 5 Hill-Rom Services Pte, Ltd. 5 Hill-Rom Manufacturing, Inc. 4 Hill-Rom Holdings, Inc. 1 Hill Engineering 1 Hill, Farrer & Borrill 1 Hill-Rom Services Private Limited 1 Hill Top Research, Inc. 1

Hill-Med, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Hill-Med”