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Perrigo New York, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 2450054

Devices
1
Registrations
FDA
FDA recalls
0

Catalogue1

Newest first, rows 1-1 of 1

  • Personal Lubricating Jelly Ref K180923

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

Company details

FDA FEI number
2450054
Address
1700 Bathgate Ave, BRONX, NY, 10457

Frequently asked questions

How many devices does PERRIGO NEW YORK, INC. have in the registry?

The registry currently lists 1 device for PERRIGO NEW YORK, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list PERRIGO NEW YORK, INC.'s devices?

Among its 1 most recently registered device, PERRIGO NEW YORK, INC. has devices listed in FDA 510(k) (1 device).

What risk classes do PERRIGO NEW YORK, INC.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for PERRIGO NEW YORK, INC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from PERRIGO NEW YORK, INC. in the registry?

The most recently registered devices listed for PERRIGO NEW YORK, INC. include Personal Lubricating Jelly.

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.