FDA applicant

Regulatory Consultants TO the Medical Device Indus

Sandy, UT1 decision1994–19940 recalls

FDA records 1 decision for Regulatory Consultants TO the Medical Device Indus (Sandy, UT) in 1994: 1 510(k) clearance. All are in product code KPX (Changer, Radiographic Film/Cassette). 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, radiology panel, where it files most

How often FDA has decided Regulatory Consultants TO the Medical Device Indus’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Regulatory Consultants TO the Medical Device Indus since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Regulatory Consultants TO the Medical Device Indus by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Regulatory Consultants TO the Medical…’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 “Regulatory”

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

Regulatory & Marketing Services, Inc. 21 Regulatory Insight, Inc. 4 Regulatory Management Services 3 Regulatory Technology Services, LLC 2 Regulatory Associates, Inc. 1 Regulatory Specialists, Inc. 1 Regulatory and Marketing Services, Inc. 1 Regulatory Strategies, Inc. 1

Regulatory Consultants TO the Medical Device Indus

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Regulatory”