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Ani Safety, Inc.

United StatesFDA applicant, unverified

Devices
2

What Ani Safety, Inc. makes

Ani Safety, Inc. manufactures emergency response safety kits and body fluids barrier kits designed for medical and public safety use. These products include protective gear and containment solutions to mitigate exposure risks in high-risk environments.

The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The products are listed in the FDA’s 510(k) database. Ani Safety, Inc. is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Emergency Response Safety Kit Ref K946001

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Body Fluids Barrier Kit Ref K944545

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Ani Safety, Inc. have in the registry?

The registry currently lists 2 devices for Ani Safety, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ani Safety, Inc.'s devices?

Among its 2 most recently registered devices, Ani Safety, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Ani Safety, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Ani Safety, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Ani Safety, Inc. in the registry?

The most recently registered devices listed for Ani Safety, Inc. include EMERGENCY RESPONSE SAFETY KIT and BODY FLUIDS BARRIER KIT.

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