20 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Moore Park Mask
FDA 510(k)
FDA Class 2
·Anesthesiology
Vanguard® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304271432·
ZenFlex CM
FDA UDI
Kerr Corporation·00195062145506·.20/.04/31mm ZenFlex CM NiTi FILE REFILL PACK
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071150839·18F x 3.5cm MiniSPC Low Profile Suprapubic Cath...
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071148218·18F x 3.5cm MiniSPC Low Profile Suprapubic Cath...
AFFIRM BREAST BIOPSY GUIDANCE SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
FLUID-FILLED TEETHER
FDA 510(k)
FDA Class 2
·Dental
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020283·
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020252·
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020214·
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020177·
TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·May 31, 2019
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 18, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013
PEG THREADED 4.0X35.0MM
FDA Adverse Event
Malfunction
·DEPUY ACE S.A.'R.L.·Product code LXT·June 22, 2011
WALTER LORENZ TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code LZD·August 29, 2017
T2 STRATOSPHERE
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code MQP·July 1, 2020
MIDAS REX MR8
FDA Adverse Event
Malfunction
·MDT POWERED SURGICAL SOLUTIONS·Product code HBC·May 9, 2025
BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HWC·June 3, 2016
MOTOR MR8 ELECTRIC
FDA Adverse Event
Malfunction
·MDT POWERED SURGICAL SOLUTIONS·Product code HBB·February 24, 2022