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Retroperc, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 3019946783

Devices
1
Registrations
FDA
FDA recalls
0

What Retroperc, Inc. makes

RetroPerc, Inc. manufactures nephrostomy introduction sheaths, designed for percutaneous nephrolithotomy procedures to facilitate safe and precise access to the kidney for stone removal.

The company’s portfolio is classified under FDA Device Class II (U) and is listed in the FDA’s Unique Device Identifier (UDI) database, with operations based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
3019946783
Address
111 Town Square Pl Ste 1203, Jersey City, NJ, 07310

Frequently asked questions

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

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

Which registries list RETROPERC, INC.'s devices?

Among its 1 most recently registered device, RETROPERC, INC. has devices listed in FDA GUDID (1 device).

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

The most recently registered devices listed for RETROPERC, INC. include RetroPerc RP91-01.

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.