37 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VU CPOD INTERVERTEBRAL BODU FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
Bur PM2-70 80K diamC Ø2.3 St
FDA UDI
Bien-Air Surgery SA·17630055517088·
Sagix
FDA UDI
Preat Corporation·00842092128022·Sagix 2.2 Red Female- Increased
ILIZAROV
FDA UDI
Smith & Nephew, Inc.·03596010030535·5/8 RING 130MM COMPOSITE
HHM
FDA UDI
Oticon A/S·05707131163288·K130, MINIRITE CNB HHM
Preci-Sagix
FDA UDI
Preat Corporation·00842092119556·Sagix 2.2 Red Female- Increased (50-Pack)
Preci-Sagix
FDA UDI
Preat Corporation·00842092108833·Sagix 2.2 Red Female- Increased (6-Pack)
ULTRA DCI MODEL 5000
FDA 510(k)
FDA Class 2
·Radiology
JOE LUBE CONDOM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
AVANTAGE INLAY SIZE 50/28
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code LPH·December 15, 2016
UNKNOWN BIOMET AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017
AVANTAGE E1 INSERT DIA28 S56
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 21, 2016
UNKNOWN BIOMET AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017
G7 BISPHERICAL SHELL 50D
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·December 15, 2025
AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·June 2, 2017
VERCISE GEVIA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·April 5, 2023
TI COLLAR FOR 6MM DUAL-OPENINGIMPLANTS
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code NKB·May 9, 2013
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 24, 2011
LUMAX 340 DR-T
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO.·Product code LWS·August 5, 2008
AVANTAGE UHMWPE INSERT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·March 29, 2017