31 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699427·GENUMEDI SILVER SIZE VIII
NANOGEN
FDA 510(k)
FDA Class 2
·Dental
DURAVENT
FDA UDI
Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948005462·DURAVENT UNI 1 IC + 1 ICU, SIZE 8
REPICCI II RESURFACING KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304447066·
VISICOIL MR
FDA UDI
Izi Medical Products, LLC·EIBASNMR03501022080·0.35mm x 1.0cm VISICOIL MR Platinum loaded into...
VISICOIL MR
FDA UDI
Izi Medical Products, LLC·B887SNMR03501022080·0.35mm x 1.0cm VISICOIL MR Platinum loaded into...
IMC SURGICAL DRAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ACCESS THYROGLOBULIN ANTIBODY AND CALIBRATORS ON THE ACCESS IMMUNOASSAY SYSTEMS, MODELS 33890, 33895
FDA 510(k)
FDA Class 2
·Immunology
Plateau Spacer System
FDA UDI
Life Spine, Inc.·00190837026059·PLATEAU Interbody, Straight, Bulleted, 10mm 22m...
LUX Expandable Interbody System
FDA UDI
XENIX MEDICAL LLC·00840493415956·Lumbar Expandable, 10x22x8-12mm, 8 Deg
LUX Expandable Lumbar Interbody System
FDA UDI
XENIX MEDICAL LLC·00840493415949·Lumbar Expandable, 10x22x8-12mm, 0 Deg
PRLNE BLU 30IN 6-0 D/A C-1
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAW·March 28, 2025
PRLNE BLU 30IN 6-0 D/A C-1
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAW·March 28, 2025
PRLNE BLU 30IN 6-0 D/A C-1
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAW·March 28, 2025
EPIPHANY
FDA UDI
PANTHEON SPINAL, LLC·B528100206021022080·#6 40 DEGREE CURVED UP CURETTE SHAFT
GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246785159·
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246785050·
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·May 9, 2013
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code MTA·September 19, 2014