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Henke Sass Wolf Of America, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1000120548

Devices
9
Registrations
FDA
FDA recalls
0

What Henke Sass Wolf Of America, Inc. makes

HENKE SASS WOLF OF AMERICA, INC. manufactures a range of endoscopic and laparoscopic devices, including saphenous vein laparoscopes, nasopharyngoscopes, arthroscopes, sinuscopes, hystero-resectoscopes with various electrodes, and bariatric laparoscopes.

The company's devices are all classified as Class II and listed in the FDA 510(k) registry. HENKE SASS WOLF OF AMERICA, INC. is based in the US.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

Company details

FDA FEI number
1000120548
Address
135 Schofield Ave, DUDLEY, MA, 01571

Frequently asked questions

How many devices does HENKE SASS WOLF OF AMERICA, INC. have in the registry?

The registry currently lists 9 devices for HENKE SASS WOLF OF AMERICA, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list HENKE SASS WOLF OF AMERICA, INC.'s devices?

Among its 9 most recently registered devices, HENKE SASS WOLF OF AMERICA, INC. has devices listed in FDA 510(k) (9 devices).

What risk classes do HENKE SASS WOLF OF AMERICA, INC.'s devices fall under?

Among its 9 most recently registered devices, the classes recorded for HENKE SASS WOLF OF AMERICA, INC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from HENKE SASS WOLF OF AMERICA, INC. in the registry?

The most recently registered devices listed for HENKE SASS WOLF OF AMERICA, INC. include HENKE SASS WOLF SAPHENOUS VEIN LAPAROSCOPE, HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE, HENKE SASS WOLF OF AMERICA ARTHROSCOPE and SINUSCOPE AND ACCESSORIES.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.