29 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HANSATOME MICROKERATOME
FDA 510(k)
FDA Class 1
·Ophthalmic
Avitene
FDA UDI
Davol Inc.·00801741010491·EndoAvitene Microfibrillar Collagen Hemostat in...
Silverbolt/Mainframe
FDA UDI
Choice Spine, LP·10885862163486·
CORTICAL SCREW 3.5mm x 26.0mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665019698·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0100600·Caddie, Modular Bone Screws
RITA STARBURST XLI ELECTROSURGICAL DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ALLROUND 55 LF
FDA 510(k)
FDA Class 2
·Dental
M-SERIES DC POWER SUPPLY
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·May 25, 2012
REMSTAR AUTO M SERIES
FDA Adverse Event
Injury
·RESPIRONICS, INC.·Product code BZD·April 14, 2024
OPTETRAK LOGIC KNEE COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 18, 2025
AXSYM DIGOXIN III
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·March 12, 2013
3M IOBAN ANTIMICROBIAL INCISE DRAPE
FDA Adverse Event
3M COMPANY·Product code KKX·February 25, 2011
LOGIC TIBIA PS MOD INSRT SZ 6 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 24, 2024
LOGIC KNEE COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 7, 2026
LOGIC TIBIA PS MOD INSRT SZ 6 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 17, 2023
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 1, 2024
LOGIC TIBIA PS MOD INSRT SZ 6 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 17, 2024
MENTOR SMOOTH ROUND HIGH PROFILE
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·June 22, 2018
LOGIC TIBIA PS MOD INSRT SZ 6 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 8, 2023