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Adept-Med Intl., Inc.

Country not established FDA establishment FEI 3000718212

Devices
6
Registrations
FDA
FDA recalls
0

What Adept-Med Intl., Inc. makes

ADEPT-MED Intl., Inc. manufactures surgical retractors, including the Goott Multipurpose Flexible Retractor and Goott Balfour Blade, designed for general and abdominal procedures. Their portfolio also includes the Adams Breast Implant Protector for surgical site protection and the Visecera Retainer and McNealy-Glassman Visecera Retainer for tissue management. The Gravespec is listed as part of their surgical instrument offerings.

The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory clearance supported through 510(k) submissions. These products are intended for use in the United States and are listed in the FDA’s 510(k) database. The manufacturer is based in the US.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue6

Newest first, rows 1-6 of 6

Company details

FDA FEI number
3000718212
Address
665 PLEASANT VALLEY ROAD, DIAMOND SPRINGS, CA, 95619

Frequently asked questions

How many devices does ADEPT-MED INTL., INC. have in the registry?

The registry currently lists 6 devices for ADEPT-MED INTL., INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list ADEPT-MED INTL., INC.'s devices?

Among its 6 most recently registered devices, ADEPT-MED INTL., INC. has devices listed in FDA 510(k) (6 devices).

What risk classes do ADEPT-MED INTL., INC.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for ADEPT-MED INTL., INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from ADEPT-MED INTL., INC. in the registry?

The most recently registered devices listed for ADEPT-MED INTL., INC. include GOOTT MULTIPURPOSE FLEXIBLE RETRACTOR (STERILE), ADAMS BREAST IMPLANT PROTECTOR, GOOTT BALFOUR BLADE and VISECERA RETAINER.

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.