36 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Distal Elbow Plating System
FDA 510(k)
FDA Class 2
·Orthopedic
Excelsior XT-17 Flex
FDA UDI
Stryker Corporation·07613252714910·2 Tip Pre-Shaped 90 Microcatheter
Ophthalmic Ring
FDA UDI
KATENA PRODUCTS, INC.·00841668100769·FLIERINGA FIXATION RING 15MM
Malibu
FDA UDI
Seaspine Orthopedics Corporation·10889981140243·Angled hook, 5.5 x9.0mm, right
Ophthalmic Ring
FDA UDI
KATENA PRODUCTS, INC.·00841668100806·FLIERINGA FIXATION RING 19MM
Canaveral®
FDA UDI
FLOSPINE LLC·B183117150900·Closed Screw Assembly, 10.5mm x 90mm
THERMA-CURE
FDA 510(k)
FDA Class 2
·Dental
DIGITAL FLAT PANEL X-RAY DETECTOR
FDA 510(k)
FDA Class 2
·Radiology
SACRO-ILIAC SCREW SYSTEM SI-JOINT SCREW 10X55
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code OUR·October 8, 2019
REFOBACIN BONE CEMENT R 1X40-3
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·March 30, 2026
REFOBACIN BONE CEMENT R 1X40-3
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·February 24, 2026
OPTIPAC 80 REFOB PLUS BONE CMT-3
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2026
CLICKX LOCKCAP F/498.571 TAN
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code MNH·June 15, 2013
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·July 21, 2011
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - GUANGZHOU·Product code KDI·October 14, 2014
REFOBACIN BONE CEMENT R 2X40G
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code MBB·March 12, 2026
REFOBACIN BONE CEMENT R 2X20-3
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·February 11, 2026
REFOBACIN BONE CEMENT R 2X40G
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·February 20, 2026
OPTIPAC 80 REFOB BONE CMT R-3
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LOD·November 14, 2025
REFOBACIN BONE CEMENT R 1X40-3
FDA Adverse Event
Death
·BIOMET FRANCE S.A.R.L.·Product code MBB·December 15, 2025