FDA applicant

Enochs Mfg., Inc.

Indianapolis, IN1 decision1988–19880 recalls

FDA records 1 decision for Enochs Mfg., Inc. (Indianapolis, IN) in 1988: 1 510(k) clearance. All are in product code LGX (Table, Examination, Medical, Powered). 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 Enochs Mfg., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Enochs Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Enochs Mfg., Inc.

Which product codes does it file in?

What has FDA decided for it lately?