Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “S128 Anterior Lumbar Interbody Fusion (ALIF) System”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED FDA 510(k) incl. De Novo 3 FDA PMA GUDID

Country / market United States 3

Risk class Class I Class IIa Class IIb Class III Class II (US) 3

More classes (11)

Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

Verified Verified only

Category (EMDN)

Browse by category

3 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

S128 Anterior Lumbar Interbody Fusion (ALIF) System

Renovis Surgical Technologies, Inc.,FDA registration: United States Group of variants

Active Regimes: 510(k) Registry: 510(k) Class:II
S128 Anterior Lumbar Interbody Fusion (Alif) System

Renovis Surgical Technologies, LLC,FDA registration: United States

Active Regimes: 510(k) Registry: 510(k) Class:II

Previous Next

Showing 1-3 of 3

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site