FDA applicant

Pymah Corp., Ati Div.

North Hollywood, CA3 decisions1989–19900 recalls

FDA records 3 decisions for Pymah Corp., Ati Div. (North Hollywood, CA) from 1989 to 1990: 3 510(k) clearances. All are in product code FRC (Indicator, Biological Sterilization Process). 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 hospital panel, where it files most

How often FDA has decided Pymah Corp., Ati Div.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pymah Corp., Ati Div. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Pymah”

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

Pymah Corp. 17

Pymah Corp., Ati Div.

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?

Other applicant names beginning “Pymah”