FDA applicant

Mehl/Group Marketing

Budd Lake, NJ1 decision1997–19970 recalls

FDA records 1 decision for Mehl/Group Marketing (Budd Lake, NJ) in 1997: 1 510(k) clearance. All are in product code KCX (Epilator, High Frequency, Tweezer-Type). Its devices cite 1 predicate, 0 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 Mehl/Group Marketing’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mehl/Group Marketing since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mehl/Group Marketing by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Mehl/Group Marketing’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 “Mehl/Group”

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

Mehl/Biophile Intl., Inc. 2 Mehl, Thomas L. 1

Mehl/Group Marketing

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Mehl/Group”