FDA applicant

Inman Medical Corp.

Fort Worth, TX14 decisions1991–19942 recalls

FDA records 14 decisions for Inman Medical Corp. (Fort Worth, TX) from 1991 to 1994: 14 510(k) clearances. Most are in product codes GCY (Apparatus, Suction, Single Patient Use…) and FRO (Dressing, Wound, Drug). 2 recalls are 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 Inman Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inman Medical Corp. since 2007.

Recalls per year

2in 2022

2007high 2 (2022) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Inman Medical 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 Liebelt Corp. 6 Inman Orthodontic Laboratories, Inc. 1

Inman Medical Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Inman”