20 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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7MM EXTENDED LENGTH ENDOSCOPE,DISSECTION TIPS, MODELS VH-1111, VH-1114
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BOM 7MM EXTENDED LENGTH ENDOSCOPE
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR LLC·Product code GCJ·March 27, 2019
Rutner
FDA UDI
COOK INCORPORATED·00827002145405·Rutner Balloon Dilation Helical Stone Extractor
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0142000·Assembly, T-Handle, T15 Split Tip Cross Connector
ThermaGuide Cannula for Cellulaze, 250mm
FDA UDI
Cynosure, LLC·00841494100469·ThermaGuide Cannula for Cellulaze, 250mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361013501·Quad Thread Cannulated Ø6x50
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0142100·Trial, TLIF, 32L OB CRV 7Deg, 10mm
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197256322·ALLIS Tissue Forceps
255mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197043441·Standard Dressing Forceps
delica...
VITROS IMMUNODIAGNOSTIC PRODUCTS HBSAG CONTROLS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
TETRIC CERAM HB
FDA 510(k)
FDA Class 2
·Dental
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 6, 2013
TENDRIL SDX
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·March 12, 2008
PERCUFLEX URETERAL STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·February 14, 2024
5.0MM TROCAR 210MM
FDA Adverse Event
Malfunction
·SYNTHES HAGENDORF·Product code FZX·January 16, 2015
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·January 14, 2015
DeVilbiss Model DV5x Series CPAP units. For use in treating Obstructive Sleep Apnea (OSA) by means of application of positive air pressure. Used in home and clinical environments.
FDA Enforcement
Class III
·Terminated·DeVilbiss Healthcare LLC·July 9, 2014
CADD-Solis Ambulatory Infusion Pumps, Model 2100. Intended for the following uses: Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a continuous rate of infusion, intermittent bolus, and/or with patient-controlled demand doses.
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·August 14, 2024
Various Hip systems, Item Nos. 104207 104212 104215 11-162809 11-162810 11-162811 11-162812 11-162813 21-103202 21-103203 21-103204 21-103205 21-103206 21-103207 21-103208 21-103209 21-103210 21-103211 21-103212 21-103215 21-104109 21-104110 21-104111 21-104112 21-104113 21-104114 21-104115 21-104116 21-104117 21-104118 21-104119 21-108110 21-108112 21-108115 21-108117 21-108119 21-108130 21-108132 21-108135 21-108137 21-108139 21-108150 21-108152 21-108155 21-108157 21-108159 21-108251 21-108253 21-108255 21-108257 21-108259 21-108271 21-108273 21-108275 21-108277 21-108279 21-108291 21-108293 21-108295 21-108297 21-108299 21-108391 21-108393 21-108395 21-108397 21-108399 21-109256 21-109260 21-109264 21-109268 21-109272 21-123202 21-123203 21-123204 21-123205 21-123206 21-123207 21-123208 21-123209 21-123210 21-123211 21-123212 21-124309 21-124310 21-124311 21-124312 21-124313 21-124314 21-124315 21-124316 21-124317 US157338 US157340 US157342 US157344 US157346 US157348 US157350 US157352 US157354 US157356 US157358 US157359 US157360 X21-180307 X21-180308 X21-180309 X21-180310 X21-180311 X21-180312 X21-180313 X21-180314 X21-180315 X21-180316 X21-180317 X21-180318 X21-180319 X21-180320 X21-180321 X21-182308 X21-182309 X21-182310 X21-182311 X21-182312 X21-182313 X21-182314 X21-182315 X21-182316 X21-182317 X21-182318 X21-182319 X21-182320 X21-182321 Product Usage: Hip arthroplasty.
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·December 4, 2019