412 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
APTUS PROXIMAL HUMERUS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Cavitron®
FDA UDI
Dentsply Professional·D00361201081·Classic P Ultrasonic Insert 25K P-10
ACRY SMART DIGITAL
FDA UDI
DENTAL MANUFACTURING SPA·08056865152400·
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756612333·Wrist Splint
DURAVENT
FDA UDI
Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948006766·DURAVENT XL 1 IC, SIZE 8
Stryker
FDA UDI
Provision·B504OM5120108150·
NA
FDA UDI
STRYKER CORPORATION·04546540077929·1.0mm Drill Bit w/8.0mm Stop
NA
FDA UDI
STRYKER CORPORATION·07613153093930·1.7mm Drill Bit w/11.6mm Stop
NA
FDA UDI
STRYKER CORPORATION·04546540077936·1.5mm Drill Bit w/8.0mm Stop
NA
FDA UDI
STRYKER CORPORATION·04546540077950·2.5mm Drill Bit w/8.0mm Stop
NA
FDA UDI
STRYKER CORPORATION·04546540077943·2.0mm Drill Bit w/8.0mm Stop
CLICKFINE PEN NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
AMEDICA DRUG TEST THC, COC, OPI, AMP, MET, PCP, BAR, BZO, MDMA, OXY, TCA
FDA 510(k)
FDA Class 2
·Clinical Toxicology
REAMER SHAFT, MOD, TRINKLE 8.0X284 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code HWE·February 13, 2012
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 20, 2013
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·May 26, 2011
SIMPULSE SOLO
FDA Adverse Event
Malfunction
·DAVOL INC., SUB. C.R. BARD, INC.·Product code FQH·August 14, 2008
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 19, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code NJR·April 17, 2026