32 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Collagen Dental Wound Dressings
FDA 510(k)
FDA Unclassified
·Unknown
Column, Sodasorb Disposable, 5.75" L
FDA UDI
A-M SYSTEMS, LLC·00817081026047·Column, Sodasorb Disposable, Prefilled, 5.75" L
CARBON FIBER ROD, Ø9.5mm x 600mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665005455·
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100431·LANCASTER EYE SPECULUM SOLID
UniTip Catheter
FDA UDI
Unisensor AG·07640172972397·
UniTip Catheter
FDA UDI
Unisensor AG·07640172972403·
DELUXE 18G MICRO CANNULA SET
FDA UDI
The Wells Johnson Company·B458201526000·Cannula Set, Deluxe 18g Micro Cannula Set, cont...
II Ring Retractor
FDA UDI
Automated Medical Products Corp.·00810118341465·Malleable Retractor 4" x 10" with Protective Edge
ZIMMER DENTAL HEX-LOCK PREPARED ABUTMENT (STRAIGHT & ANGLED)
FDA 510(k)
FDA Class 2
·Dental
SIMPLYGO BREAST PUMP
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 10, 2020
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·March 26, 2021
LIFEPAK(R) 1000 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015
DEPUY SYNTHES UNIVERSAL HANDLE
FDA Adverse Event
Injury
·DEPUY SYNTHES·Product code LXH·October 2, 2014
AGILIS NXT, 8.5F, STEERABLE INTRODUCER, MED CURL
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC. (AF-MINNETONKA)·Product code DYB·June 5, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 27, 2011
CD HORIZON® FENESTRATED SCREW SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·September 3, 2024
LIFEPAK® 1000 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·April 24, 2019
CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NKB·July 28, 2025
CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NKB·July 28, 2025