32 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PROCELLERA
FDA 510(k)
FDA Unclassified
·Unknown
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169604803·SPACER 2130350 OLIF25 27MM 0 DEG 12X50
ArgenZ HT+ 98x18 ML A1B
FDA UDI
ARGEN CORPORATION, THE·D818130350·Dental porcelain/ceramic restoration kit
Shoulder retr. for LEPS™,set/2
FDA UDI
MACROMEDICS B.V.·08719425702339·Shoulder retractor for use with LEPS, set of 2
AquaMic™ 3D Color Cap
FDA UDI
Advanced Bionics, LLC·00840094452985·Resin Black
AquaMic™ 3D Color Cap
FDA UDI
Advanced Bionics AG·07630016861673·Resin Black
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981176044·Z-Rod, Dia. 6.0mm, Titanium, 350mm
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780433309·Integra® Jarit® Potts-Smith Forceps, Dressing, ...
EXPRESS MINI GLAUCOMA SHUNT
FDA 510(k)
FDA Class 2
·Ophthalmic
HOVEROUND TEKNIQUE GT POWER WHEELCHAIR, MODEL# TEKNIQUE GT
FDA 510(k)
FDA Class 2
·Physical Medicine
Kalitec Universal Instruments
FDA UDI
Kalitec Direct LLC·B07301K1103500·Tray, Base, 3.5", Arcamed
T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·May 28, 2020
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·August 31, 2023
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·September 2, 2022
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·October 26, 2022
Truliant
FDA UDI
Exactech, Inc.·10885862314710·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024494626·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024494633·
ULTRAPEN REUSABLE PENCIL, MODEL 130350 THROUGH 130353, REUSABLE ACCESSORY ELECTRODE KIT (FOR USE WITH ULTRAPEN PENCIL),
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PROCEDURAL STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM DE MEXICO S DE RL DE CV·Product code FPO·March 12, 2013