FDA applicant

The Altomec Corp.

Torrance, CA2 decisions1998–19990 recalls

FDA records 2 decisions for The Altomec Corp. (Torrance, CA) from 1998 to 1999: 2 510(k) clearances. All are in product code GCJ (Laparoscope, General & Plastic Surgery). 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 The Altomec Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Altomec Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “The”

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

Altomec Endoscopy, Inc. 1

The Altomec Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”