27 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SNaP Wound Care System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089476701·
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089476862·
STILLE Osteotomes
FDA UDI
Stille AB·07332339211486·OSTEOTOME CINELLI STILLE double-guarded 10 mm 1...
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100219·LIEBERMAN ASPIRATING SPECULUM K-WIRE
LUXATEMP ULTRA /STAR
FDA 510(k)
FDA Class 2
·Dental
THERMAGE THERMACOOL COUPLING FLUID
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PU-681RA
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·September 12, 2023
PU-681RA
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·July 14, 2023
C-PLUS™* PEEK VBR/IBF SYSTEM
FDA UDI
Pioneer Surgical Technology, Inc.·00846468031343·14.5 X 17 X 10MM C-PLUS, VBR
C-Plus PEEK IBF System
FDA UDI
Pioneer Surgical Technology, Inc.·00846468033644·INTERBODY FUSION DEVICE
Fortilink-C IBF System
FDA UDI
Pioneer Surgical Technology, Inc.·00191083006673·Interbody Fusion Device
Fortilink®-C IBF System
FDA UDI
Xtant Medical Holdings, Inc.·00840311212903·Fortilink-C, 14.5x17, 10mm, 6L
Fortilink-C
FDA UDI
Pioneer Surgical Technology, Inc.·00846468080457·FORTILINK-C Tetrafuse 14.5x17 10mm, 6L
CARELINK
FDA Adverse Event
Malfunction
·RICE CREEK MFG·Product code DXY·June 7, 2013
VITALITY
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 6, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 10, 2008
ATTUNE CRS RP INSRT SZ 7 12MM
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code NJL·October 7, 2022
D902 LILLIPUT ECMO M PHISIO
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·April 7, 2022
LILLIPUP PMP, LILLIPUT PMP INTEGRATED
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·June 27, 2022