32 results · 21ms · Sources: EU EUDAMED, US FDA

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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