84 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CONCENPIECE,HIGH-SPEED HANDPIECE SERIES
FDA 510(k)
FDA Class 1
·Dental
Mini Twin
FDA UDI
Rmo, Inc.·00885797652775·ROTH MINI LP 018 HK/3 5-5 20EA
Oticon
FDA UDI
Oticon A/S·05707131233929·K5, BTE 13 STG
Pilot Spinal System
FDA UDI
Life Spine, Inc.·00190837051358·Pilot Rod Hex Driver
CapSure® Spine System
FDA UDI
Spine Wave, Inc.·10840642104516·Rod Straight 5.5 x 300mm
SILO
FDA UDI
AURORA SPINE, INC.·B5211133010·SILO, MIS TUBE
Innomed, Inc.
FDA UDI
INNOMED, INC.·00840277118448·Llinas Leg Length & Lateral Offset Gauge
Innomed, Inc.
FDA UDI
INNOMED, INC.·00840277109095·Adjustable Standard 3.2mm Measuring Pin
SILK'N FX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
UNI-T SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·September 13, 2019
UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022
UNKNOWN
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 23, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code CAW·September 24, 2014
DELTA CER HEAD 12/14 32MM +1
FDA Adverse Event
Injury
·DEPUY INTL., LTD.·Product code LZO·May 20, 2011
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·February 6, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 35
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code HWC·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 40
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019