20 results · 48ms · Sources: EU EUDAMED, US FDA

IdentiTi NanoTec

FDA registration
Sterigenics US, LLC·3 products·🇺🇸 United States

IdentiTi Porous Ti Interbody System

FDA registration
Alphatec Spine, Inc.·3 products·🇺🇸 United States

IdentiTi Porous Ti Interbody System

FDA registration
ALPHATEC SPINE, INC.·3 products·🇺🇸 United States

LIF AMP, Bone Screw X2

FDA registration
PACKAGING COMPLIANCE MEDICAL, LLC·2 products·🇺🇸 United States

IdentiTi NanoTec

FDA registration
Sterigenics US LLC·3 products·🇺🇸 United States

IdentiTi™ Porous Ti Interbody System, IdentiTi™ NanoTec™ Interbody System, Transcend™ PEEK Interbody System, Transcend™ NanoTec™ Interbody System, IdentiTi™ ALIF Standalone Interbody System, IdentiTi™ NanoTec™ ALIF Standalone Interbody System

FDA 510(k)
FDA Class 2 ·Orthopedic

HEALIX ADVANCE PEEK ANCHOR w/DYNACORD

FDA UDI
Medos International Sàrl·10886705029426·HEALIX ADVANCE PEEK ANCHOR w/DYNACORD PEEK Anch...

FAC-4 - Class B 21 White Cap - 4 Shelf Cabinet

FDA UDI
Certified Safety Manufacturing, Inc.·00766588620282·FAC-4 - Class B 21 White Cap - 4 Shelf Cabinet

Type 1053 - FreeFit

FDA registration
Natus Medical Denmark ApS·1 product·🇩🇰 Denmark

Reference microphone

FDA registration
Natus Manufacturing Limited·1 product·🇮🇪 Ireland

Dermalux Flex MD

FDA registration
AESTHETIC TECHNOLOGY LTD·4 products·🇬🇧 United Kingdom

CentriMag Blood Pump, CentriMag Acute Circulatory Support System

FDA registration
Thoratec Switzerland GMBH·1 product·🇨🇭 Switzerland

Nightowl

FDA registration
RESMED CORP·1 product·🇺🇸 United States

CentriMag™ Blood Pump for use with CentriMag™ Acute Circulatory Support System

FDA registration
APPLIMED SA -CSSR·1 product·🇨🇭 Switzerland

MEDISONO, LLC

FDA registration
MEDISONO, LLC·3 products·🇺🇸 United States

AURICAL HIT

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

VX-400 TOPICAL HYPERBARIC OXYGEN CHAMBER

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Chamber, Oxygen, Topical, Extremity

FDA classification
FDA Class 2 ·Chamber, Oxygen, Topical, Extremity

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification
FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Calibrator, Hearing Aid / Earphone And Analysis Systems

FDA classification
FDA Class 2 ·Calibrator, Hearing Aid / Earphone And Analysis Systems