FDA applicant

Pymah Corp.

Somerville, NJ17 decisions1988–19960 recalls

FDA records 17 decisions for Pymah Corp. (Somerville, NJ) from 1988 to 1996: 17 510(k) clearances. Most are in product codes JOJ (Indicator, Physical/Chemical Sterilization…) and DXQ (Blood Pressure Cuff). 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.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pymah Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pymah 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 “Pymah”

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

Pymah Corp., Ati Div. 3

Pymah 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?

Other applicant names beginning “Pymah”