FDA applicant

Regulatory & Marketing Services, Inc.

Palm Harbor, FL21 decisions1993–19960 recalls

FDA records 21 decisions for Regulatory & Marketing Services, Inc. (Palm Harbor, FL) from 1993 to 1996: 21 510(k) clearances. Most are in product codes EZL (Catheter, Retention Type, Balloon) and FGM (Probe And Director, Gastro-Urology). 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 Regulatory & Marketing Services, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Regulatory & Marketing Services, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Regulatory”

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

Regulatory Insight, Inc. 4 Regulatory Management Services 3 Regulatory Technology Services, LLC 2 Regulatory Associates, Inc. 1 Regulatory Specialists, Inc. 1 Regulatory Consultants TO the Medical Device Indus 1 Regulatory and Marketing Services, Inc. 1 Regulatory Strategies, Inc. 1

Regulatory & Marketing Services, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Regulatory”