17 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FAMILY OF COOLGLIDE AESTHETIC LASERS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PROFILE LITE 2
FDA UDI
Respironics, Inc.·00606959044180·Profile Lite 2 SE with Headgear, Large, Italy
Reef TO
FDA UDI
Seaspine Orthopedics Corporation·10889981204907·Trial, 11mm x 32mm x 18mm, 15 Deg
Reef TH
FDA UDI
Seaspine Orthopedics Corporation·10889981201050·Interbody, 11mm x 32mm x 18mm, 15 deg
Reef TO
FDA UDI
Seaspine Orthopedics Corporation·10889981190750·Interbody, 11mm x 32mm x 18mm, 15 Deg
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981193065·Interbody, 11mm x 32mm x 18mm, 15 deg
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981208172·Trial, 11mm x 32mm x 18mm, 15 deg
FOURSNARE VASCULAR RETRIEVAL SNARE
FDA 510(k)
FDA Class 2
·Cardiovascular
U-MOTION II ACETABULAR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TURBO-JECT® DOUBLE LUMEN POWER-INJECTABLE PICC
FDA Adverse Event
Injury
·COOK INC·Product code LJS·December 3, 2015
AEQUALIS REVERSED BASE PLATE TA6V LONG PEG WITH HA
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·April 19, 2023
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 29, 2025
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013
RADIESSE DERMAL FILLER
FDA Adverse Event
Other
·MERZ AESTHETIC, INC.·Product code LMH·June 7, 2011
530G INSULIN PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·October 1, 2014
NAIL, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code JDS·April 16, 2014
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·April 14, 2014