911 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Peridot Intervertebral body fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
Bernafon
FDA UDI
Bernafon AG·05711584087008·ZR3, KIT 13 NFM R BE ZERENA 3
OsteoMed
FDA UDI
OSTEOMED LLC·00845694015363·2.0mm x 26mm Cannulated Lag Screw
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776199913·Lletz WGraves R L ET
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070324·Cannulated 2.0 x 26mm Lag Screw Sterile Qty 5
EASYCARE TX, TX LINK
FDA 510(k)
FDA Class 2
·Anesthesiology
SEASPINE SPACER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 3, 2026
STRYKEFLOW
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY·Product code GCX·April 25, 2025
PINNACLE SECTOR II CUP 50MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWA·October 6, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011
ALIGN TO URETHRAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·BARD SHANNON LIMITED·Product code OTN·June 20, 2013
MEDLINE
FDA Adverse Event
Malfunction
·MEDLINE INDUSTRIES, LP·Product code FDE·March 20, 2026
CADD CASSETTE 100ML W/FLOWSTOP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC·Product code LHI·March 10, 2022
CADD CASSETTE 100ML W/FLOWSTOP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code LHI·March 10, 2022
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 15, 2026
EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE
FDA Adverse Event
Malfunction
·SHIRAKAWA OLYMPUS CO., LTD.·Product code ODG·April 25, 2026
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 21, 2026
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·February 26, 2026
SERRANATOR PTA SERRATION BALLOON CATHETER
FDA Adverse Event
Malfunction
·CAGENT VASCULAR, LLC·Product code PNO·February 14, 2024