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Pymah Corp.

United StatesFDA 510(k) applicant, unverified

Devices
17

What Pymah Corp. makes

Pymah Corp. manufactures ethylene oxide sterilization indicators and test packs, including disposable and reusable options for monitoring gas and steam sterilization processes. Their portfolio also includes glutaraldehyde monitors for chemical sterilization, as well as pre-gaged balanced cuffs and thermometer sheaths for medical device compatibility. Additional products feature biological indicators and antimicrobial-treated components for sterile processing applications.

The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. Their products are listed in the FDA’s 510(k) registry, and the company operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Pymah Corp. have in the registry?

The registry currently lists 17 devices for Pymah Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Pymah Corp.'s devices?

Among its 17 most recently registered devices, Pymah Corp. has devices listed in FDA 510(k) (17 devices).

What risk classes do Pymah Corp.'s devices fall under?

Among its 17 most recently registered devices, the classes recorded for Pymah Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Pymah Corp. in the registry?

The most recently registered devices listed for Pymah Corp. include STERIGAGE EO 100%, ATI ETHYLENE OXIDE STERILIZATION INDICATOR, ATI DISPOSABLE TEST PACK FOR STEAM STERILIZATION and STERIGAGE INTEGRATOR TEST PACK FOR STEAM STERILI..

Generated automatically from registry data and not verified by a human reviewer.