Skip to content

Empirical Spine, Inc.

Country not established FDA establishment FEI 3013114075

Devices
11
Registrations
FDA
FDA recalls
0

Catalogue11

Newest first, rows 1-11 of 11

Search and filter all 11 devices
Skip device list

Rows 1-11 of 11

Company details

FDA FEI number
3013114075
Address
18655 Madrone Pkwy Ste 180, Morgan Hill, CA, 95037

Frequently asked questions

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

The registry currently lists 11 devices for EMPIRICAL SPINE, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list EMPIRICAL SPINE, INC.'s devices?

Among its 11 most recently registered devices, EMPIRICAL SPINE, INC. has devices listed in FDA 510(k) (1 device), FDA PMA (1 device) and FDA GUDID (9 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do EMPIRICAL SPINE, INC.'s devices fall under?

Among its 11 most recently registered devices, the classes recorded for EMPIRICAL SPINE, INC.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for EMPIRICAL SPINE, INC. include Limiflex Dynamic Sagittal Tether Gen 3, Limiflex Dynamic Sagittal Tether Instrument Set Gen 3, Passer Gen 3 and Holder Gen 3.

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.