37 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPL CRIMP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Astra
FDA UDI
Preat Corporation·00842092167281·Astra®-compatible Aqua 3.5/4.0mm Engaging Plast...
artVeneer life
FDA UDI
Merz Dental GmbH·D7092002110·artVeneer life upper posteriors, XL, C3
SCANLAN®
FDA UDI
SCANLAN INTERNATIONAL INC·00846159007817·Dennis Multi-Purpose Clamp
Golden Isles Pedicle Screw System
FDA UDI
Intelivation, LLC·G079C2520021100·Curved Cobalt Chrome Rod, Extended Hex
CorticaLINK
FDA UDI
LINKSPINE, INC.·00817329022350·CoCr Rod - Straight - 110mm
TAURUS
FDA UDI
CTL Medical Corporation·00841732163669·Taurus Pedicle Screw System-Curved Rod Ext Hex ...
Taurus Pedicle Screw System
FDA UDI
SINTX Technologies, Inc.·M555252002110·Taurus Pedicle Screw System-Curved Rod Ext Hex ...
MEDIUM 199 EBSS/NUTRIENT MIXTURE F-10 #200-2110
FDA 510(k)
FDA Class 1
·Hematology
Spex Limited
FDA UDI
SPEX LIMITED·09420051794627·Spex Fixed Thigh Support, Seat Pan Mount, Quick...
Spex Limited
FDA UDI
SPEX LIMITED·09420051794634·Spex Fixed Thigh Support, Seat Pan Mount, Quick...
CRYSTAL-EEG MODEL 15
FDA 510(k)
FDA Class 2
·Neurology
HI-RES 9000 PHASED ARRAY CAROTID COIL
FDA 510(k)
FDA Class 2
·Radiology
SLEEPEASY
FDA Adverse Event
Injury
·RESPIRONICS INC.·Product code BZD·April 12, 2012
REMSTAR PLUS M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·May 6, 2010
REMSTAR M SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·November 25, 2009
M-SERIES DC POWER SUPPLY
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·May 25, 2012
HEYER-SCHULTEZ SALINE BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR CORP.·Product code FWM·May 19, 1994
HEYER-SCHULTE SALINE BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR CORP.·Product code FWM·May 19, 1994
HEYER-SCHULTE SALINE BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR CORP.·Product code FWM·May 19, 1994