FDA applicant

Inman Liebelt Corp.

Arlington, TX6 decisions1990–19910 recalls

FDA records 6 decisions for Inman Liebelt Corp. (Arlington, TX) from 1990 to 1991: 6 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and HDA (Forceps, Obstetrical). 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 Inman Liebelt Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inman Liebelt Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Inman Liebelt Corp.’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 “Inman”

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

Inman Medical Corp. 14 Inman Orthodontic Laboratories, Inc. 1

Inman Liebelt Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Inman”