19 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SOMATOM Definition AS/AS+
FDA 510(k)
FDA Class 2
·Radiology
CoRoent
FDA UDI
Nuvasive, Inc.·00887517575159·CoRoent Ant TLIF Ti, 14x13x40mm 0°
V. Mueller
FDA UDI
STERIS CORPORATION·10885403279249·V. Mueller DISPOSABLE BIPOLAR FORCEPS
N/A
FDA UDI
TETRA MEDICAL SUPPLY CORP.·00614138128293·ELBOW IMMOB FOAM W/STAYS, XS/INFANT
SCHWERT
FDA UDI
A. Schweickhardt GmbH & Co. KG·E89611434000·Scissors, KELLY SUPERCUT
one bl...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702472936·E3/AG/PL-OT-E/NOP5-T-OH/BLU
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702627435·ELVAREX 3/KNEE HIGH/SLANT-CLOSED TOE-ELEPHANTIA...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702253740·Elvarex 2/Thigh High/Open Toe-Elephantiasis-Ver...
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·April 14, 2022
FIXATE TISSUE BAND
FDA 510(k)
FDA Class 2
·Neurology
FLUOROMAP SOFTWARE, 9 FLUORODISC (BELT), 12 FLUORO DISC (BELT), CLOSE TUBE CLIP
FDA 510(k)
FDA Class 2
·Neurology
UNK COOLSCULPTING
FDA Adverse Event
Injury
·ALLERGAN PLEASANTON·Product code OOK·November 4, 2021
CAPSUREFIX NOVUS MRI SURESCAN
FDA Adverse Event
Injury
·MPRI·Product code DTB·May 24, 2019
UNKNOWN COOLSCULPTING SYSTEM
FDA Adverse Event
Injury
·ALLERGAN PLEASANTON·Product code OOK·June 14, 2021
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 3, 2013
530 G INSULIN PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OZO·September 27, 2014
INBONE(R) HOLDING TOOL
FDA Adverse Event
Malfunction
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HSN·June 29, 2011
SOLARICE RX
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code LOX·August 26, 2019
Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 11-114641 11-114642 11-114643 11-114644 11-114644S 11-114645 11-114646 11-114647 11-114648 11-114661 11-114662 11-114663 11-114664 11-114664S 11-114665 11-114666 11-114667 11-114668 11-114632 11-114633 Product Usage: Partial Shoulder Replacement.
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·December 4, 2019