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Shinemound Enterprise, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1221921

Devices
8
Registrations
FDA
FDA recalls
0

Catalogue8

Newest first, rows 1-8 of 8

Company details

FDA FEI number
1221921
Address
19 Sterling Rd Ste 6A, N Billerica, MA, 01862

Frequently asked questions

How many devices does SHINEMOUND ENTERPRISE, INC. have in the registry?

The registry currently lists 8 devices for SHINEMOUND ENTERPRISE, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list SHINEMOUND ENTERPRISE, INC.'s devices?

Among its 8 most recently registered devices, SHINEMOUND ENTERPRISE, INC. has devices listed in FDA 510(k) (8 devices).

What risk classes do SHINEMOUND ENTERPRISE, INC.'s devices fall under?

Among its 8 most recently registered devices, the classes recorded for SHINEMOUND ENTERPRISE, INC.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from SHINEMOUND ENTERPRISE, INC. in the registry?

The most recently registered devices listed for SHINEMOUND ENTERPRISE, INC. include LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES, SYNTEX, SENSI-PRO DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE PIGMENT ADDITIVES and SENSI-PRO DISPOSABLE POWDERED VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE PIGMENT ADDITIVES.

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.