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Trans Aire

Country not established

Devices
1

What Trans Aire makes

Trans Aire manufactures absorbable surgical sponges designed for use in medical procedures to control bleeding and absorb fluids during surgery.

The company’s products are classified as Class II (U) devices under FDA regulations and are listed in the 510(k) clearance registry. The manufacturer is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Rand Surgical Sponge Ref K971178

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

Frequently asked questions

How many devices does Trans Aire have in the registry?

The registry currently lists 1 device for Trans Aire. Devices recorded under merged duplicate company entries are counted once.

Which registries list Trans Aire's devices?

Among its 1 most recently registered device, Trans Aire has devices listed in FDA 510(k) (1 device).

What are the newest devices from Trans Aire in the registry?

The most recently registered devices listed for Trans Aire include RAND SURGICAL SPONGE.

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