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Fisher Scientific Company L.L.C.

United Statesfrom the FDA registration address FDA establishment FEI 2517925

Devices
903
Registrations
FDA
FDA recalls
0

What Fisher Scientific Company L.L.C. makes

Fisher Scientific Company L.L.C. manufactures general specimen microscopy slides, microscope slide coverslips, tissue embedding moulds, and histology tissue cassette lids, all for in vitro diagnostic use and designed as single-use products. The company also produces nitrile examination and treatment gloves that are non-powdered and non-antimicrobial, as well as reusable surgical instruments including soft-tissue manipulation forceps (tweezers-like), general-purpose surgical spatulas, and general-purpose surgical scissors.

These devices are classified as Class I and Class II medical devices and are listed in the FDA’s Unique Device Identification (FDA UDI) system. The company is based in the United States.

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

Catalogue903

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Company details

FDA FEI number
2517925
Address
300 Industry Dr, PITTSBURGH, PA, 15275

Frequently asked questions

How many devices does FISHER SCIENTIFIC COMPANY L.L.C. have in the registry?

The registry currently lists 903 devices for FISHER SCIENTIFIC COMPANY L.L.C.. Devices recorded under merged duplicate company entries are counted once.

Which registries list FISHER SCIENTIFIC COMPANY L.L.C.'s devices?

Among its 50 most recently registered devices, FISHER SCIENTIFIC COMPANY L.L.C. has devices listed in FDA GUDID (50 devices).

What risk classes do FISHER SCIENTIFIC COMPANY L.L.C.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for FISHER SCIENTIFIC COMPANY L.L.C.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from FISHER SCIENTIFIC COMPANY L.L.C. in the registry?

The most recently registered devices listed for FISHER SCIENTIFIC COMPANY L.L.C. include Fisherbrand 110711PL-FH, Fisherbrand 11002225, Fisherbrand 238017P and Fisherbrand 22X22-2-600621T.

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.