Skip to content

Fci Ophthalmics, Inc.

Country not established FDA establishment FEI 3000210020

Devices
13
Registrations
FDA
FDA recalls
0

Catalogue13

Newest first, rows 1-13 of 13

Search and filter all 13 devices
Skip device list

Rows 1-13 of 13

Company details

FDA FEI number
3000210020
Address
30 Corporate Park Drive, Pembroke, MA, 02359

Frequently asked questions

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

The registry currently lists 13 devices for FCI OPHTHALMICS, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list FCI OPHTHALMICS, INC.'s devices?

Among its 13 most recently registered devices, FCI OPHTHALMICS, INC. has devices listed in FDA 510(k) (13 devices).

What risk classes do FCI OPHTHALMICS, INC.'s devices fall under?

Among its 13 most recently registered devices, the classes recorded for FCI OPHTHALMICS, INC.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for FCI OPHTHALMICS, INC. include SNUG PLUG PUNCTUM PLUG, RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGES, PUNCTUM PLUGS & READY-SET PUNCTAL PLUGS and TITANIUM PEG SYSTEM.

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.