510(k) Report

FDA applicant

Ideal Medical, Inc.

Clearwater, FL16 decisions1981–19940 recalls

FDA records 16 decisions for Ideal Medical, Inc. (Clearwater, FL) from 1981 to 1994: 16 510(k) clearances. Most are in product codes DXE (Catheter, Embolectomy) and LQR (Dislodger, Stone, Biliary). 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 Ideal Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ideal Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ideal Medical, Inc.’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 “Ideal”

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