FDA applicant

Mahe-Medizintechnik

Nashville, TN8 decisions1993–19940 recalls

FDA records 8 decisions for Mahe-Medizintechnik (Nashville, TN) from 1993 to 1994: 8 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and LXH (Orthopedic Manual Surgical Instrument). 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 Mahe-Medizintechnik’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mahe-Medizintechnik since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mahe-Medizintechnik’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 “Mahe-Medizintechnik”

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

Mahe Intl., Inc. 3 Mahe Medical GmbH 2

Mahe-Medizintechnik

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mahe-Medizintechnik”