18 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TRAY-LINK
FDA 510(k)
FDA Class 2
·Dental
MaXcess
FDA UDI
Nuvasive, Inc.·00887517201706·MaXcess-C Retractor, Right M-L
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613327122909·2D MESH STORAGE RACK WITH LID
SCOTT'S SELECT MICROHYBRID SYRINGE 4.5 Gm (A1)
FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D77819920010·Scott’s Select Microhybrid Composite is indicat...
Coblation
FDA UDI
Smith & Nephew, Inc.·00817470004472·PERC DLR SPINE WAND SURGICAL DEVICE
COMFICARE PAD (FOR SINGEL PT USE)
FDA 510(k)
FDA Class 2
·General Hospital
Sterilucent self-Contained Biological Indicator, Sterilucent Lumen Cycle Process Challenge Device, Sterilucent Flexible Cycle Process Challenge Device
FDA 510(k)
FDA Class 2
·General Hospital
RADIFOCUS OPTITORQUE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022
ACCU-CHEK ® SPIRIT
FDA Adverse Event
Malfunction
·ROCHE DIABETES CARE AG·Product code LZG·March 7, 2013
STANDARD LOW IMPEDANCE LEAD
FDA Adverse Event
Malfunction
·MPROC, VILLALBA·Product code LGW·February 4, 2011
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014
EXACTECH
FDA Adverse Event
Malfunction
·EXACTECH, INC.·Product code LXH·April 26, 2022
OPTETRAK
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·March 27, 2019
OPTETRAK
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·March 27, 2019
OPTITORQUE ANGIOGRAPHIC CATHETER
FDA Adverse Event
Malfunction
·Product code DQO·January 20, 2021
EXACTECH
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code LXH·March 29, 2022
MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·December 12, 2022
MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 4, 2025