Endoplus

United Statesfrom the FDA registration address FDA FEI 3000719482

Devices: 913
Registrations: FDA
FDA recalls: 2

At a glance

Counted by deviCERTS from registry records

Market reach

United States: FDA FEI, FDA recalls

What Endoplus makes

Endoplus manufactures rigid endoscopic tissue manipulation forceps that are reusable.

The company's devices are classified as Class II and are listed in the FDA UDI registry. Endoplus is based in the US.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue913

Newest first, rows 1-50 of 913

Search and filter all 913 devices

Rows 1-50 of 913

Showing 1-50 of 913

Company details

FDA FEI number: 3000719482
DUNS number: 794679167
Address: 750 Tower Rd Ste A, Mundelein, IL, 60060

FDA recalls2

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 2 recalls initiated by Endoplus, initiated on 2013-07-15. By recorded status: 2 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

2013
- 15 Jul 2013 Z-2264-2013 Class II Terminated Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures. Distribution: Distributed in the states of FL, TX, and VA. Submission number: K925079
- 15 Jul 2013 Z-2265-2013 Class II Terminated Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures. Distribution: Distributed in the states of FL, TX, and VA. Submission number: K925079

Frequently asked questions

How many devices does Endoplus have in the registry?

The registry currently lists 913 devices for Endoplus. Devices recorded under merged duplicate company entries are counted once.

Which registries list Endoplus's devices?

Among its 50 most recently registered devices, Endoplus has devices listed in FDA GUDID (50 devices).

What risk classes do Endoplus's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Endoplus's devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Endoplus?

FDA recall records list 2 recalls initiated by Endoplus, the most recent initiated on 15 Jul 2013. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Endoplus in the registry?

The most recently registered devices listed for Endoplus include Endoplus E366RR-45, Endoplus E367RR-45, Endoplus E416SR-45 and Endoplus E365RR-45.

Generated automatically from registry data and not verified by a human reviewer.