90 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FDR D-EVO II FLAT PANEL DETECTOR SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
Equator
FDA UDI
Preat Corporation·00842092186664·Equator Abutment for Astra TX 3.0 x 3mm
PRINCETON
FDA UDI
Princeton Medical Group, Inc.·00810158212107·UTERINE DILATOR HEGAR DOUBLE ENDED 3/4MMØ
OsteoMed
FDA UDI
OSTEOMED LLC·00845694026437·MFx Angulated Locking BSSO Plate, 4 Hole, Short
ELMED
FDA UDI
ELMED INCORPORATED·00842180199613·laminectomy rongeur, CUSHING, 2x10mm, 12.5cm, 4...
LEONE SPA
FDA UDI
LEONE SPA·08033707010876·CALIBRA 1ST MOL BANDS W/G8025-02 n.UR 3
INFINITY TRIDENT NMT POD
FDA 510(k)
FDA Class 2
·Anesthesiology
XPRESS BALLOON DEVICE
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
MITEK, CUFFTACK ANCHOR
FDA Adverse Event
Injury
·MITEK WORLDWIDE·Product code MAI·May 6, 2003
CIRCLE "C" DUAL LUMEN CATHETER KIT
FDA Adverse Event
Malfunction
·HORIZON MEDICAL PRODUCTS, INC.·Product code KOC·February 4, 2003
PERCLOSE
FDA Adverse Event
Other
·PERCLOSE INC·Product code MGB·July 22, 2003
HELICAL BLADE COUPLING SCREW
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code LXH·March 29, 2013
TEMPORARY PACKING WIRE
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code GAO·October 20, 2004
ARTROMOT K3 (KNEE)
FDA Adverse Event
Other
·MEDIREHA GMBH·Product code BXB·June 23, 2003
RITTER
FDA Adverse Event
Malfunction
·MIDMARK CORPORATION·Product code EAZ·January 2, 2026
JOHNSON & JOHNSON ORTHOPAEDICS
FDA Adverse Event
Malfunction
·DEPUY·Product code HWC·January 29, 2003
UNKNOWN SCREWS
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code HWC·September 12, 2019
ARTHROCARE
FDA Adverse Event
Malfunction
·ARTHROCARE CORP.·Product code HRX·November 18, 2003
INTRIGUE13X145MM POLISHED STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDG·February 21, 2014
R/B RLOC LHOLE SHL 52MM SZ 23
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·February 21, 2014