FDA applicant

Dial Medical of Florida, Inc.

Palm Florida, FL2 decisions1987–19940 recalls

FDA records 2 decisions for Dial Medical of Florida, Inc. (Palm Florida, FL) from 1987 to 1994: 2 510(k) clearances. Most are in product codes FOZ (Catheter, Intravascular, Therapeutic…) and KPO (Dialysate Concentrate For Hemodialysis (Liquid…). 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 hospital panel, where it files most

How often FDA has decided Dial Medical of Florida, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dial Medical of Florida, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dial Medical of Florida, 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 “Dial”

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

Dial-X Instruments, Inc. 1 Dial Medical Supply 1 Dial-A-Rad 1

Dial Medical of Florida, 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 “Dial”