28 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EMS PIEZON MASTER 700
FDA 510(k)
FDA Class 2
·Dental
Medtronic Reusable Instruments
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00681490862707·GUIDE 9093000 BURR SPACER
RCM6
FDA UDI
COLLAGEN MATRIX, INC.·00813954027487·Resorbable Collagen Membrane
RCM6 Resorbable Collagen Membrane
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950007325·RCM6 COLLAGEN DENTAL MEMBRANE 20X30MM RESORBABL...
RCM6 Resorbable Collagen Membrane
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950008155·*SPECIAL ORDER* COLLAGEN DNTL MEMBRANE 20X30MM ...
Daily QA-MR
FDA UDI
SUN NUCLEAR CORP.·05060608880959·Radiation therapy QA device.
rf-Daily QA 3
FDA UDI
SUN NUCLEAR CORP.·05060608880171·Radiation therapy QA device.
Daily QA 3
FDA UDI
SUN NUCLEAR CORP.·05060608880034·Radiation therapy QA device.
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702274363·Elvarex 3/Thigh High/Slant, Open Toe, Knee Comf...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702658149·ELVAREX FORTE 3/KNEE HIGH/CLOSED TOE-ELEPHANTIA...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702357967·Elvarex 2/Knee High/Closed Toe-Elephantiasis-Ve...
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0130001·PLATE BENDER, UNIVERSAL
GRAMS NYLON NONABSORBABLE SUTURE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDTRONIC INVISX BURR HOLE LOCK, MODEL 60520
FDA 510(k)
FDA Class 2
·Neurology
VDW SILVER RECIPROCATING MOTOR
FDA Adverse Event
Malfunction
·DENTSPLY VDW GMBH·Product code EBW·August 14, 2019
SUMMIT POR TAPER SZ7 HI OFF
FDA Adverse Event
Injury
·DEPUY WARSAW·Product code LPH·May 3, 2013
RAD-8 HORIZONTAL
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·September 5, 2014
UNKNOWN
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·May 5, 2011
VDW SILVER RECIPROCATING MOTOR
FDA Adverse Event
Malfunction
·DENTSPLY VDW GMBH·Product code EBW·August 7, 2020
Powerlink System with IntuiTrak Delivery System (Endovascular Graft): Model Number 34-34-80LE, LOTS W09-2967 AND W09-3000.
FDA Recall
Terminated
·Endologix Inc·Product code OAD·November 25, 2009