25 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Citregen Tendon Interference Screw and Citrelock
FDA 510(k)
FDA Class 2
·Orthopedic
INTERDENTAL OSTEOTOMY OSSEO 8mm
FDA UDI
W.H. Holden, Inc.·D9282007250·
INTERDENTAL OSTEOTOMY OSSEO 4mm FLAT WITH BI-BEVEL SHARP END
FDA UDI
W.H. Holden, Inc.·D9282007252B0·
INTERDENTAL OSTEOTOMY OSSEO 8mm FLAT WITH BI-BEVEL SHARP END
FDA UDI
W.H. Holden, Inc.·D9282007251B0·
HWA (AND) SILKTEX POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (50 MICROGRAM OR LESS)
FDA 510(k)
FDA Class 1
·General Hospital
MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DE1
FDA 510(k)
FDA Class 2
·General Hospital
AUVON TENS & EMS DEVICE
FDA Adverse Event
Injury
·SHEN ZHEN AS TEC TECHNOLOGY CO LTD·Product code NUH·January 28, 2025
HAEMOLANCE LANCET
FDA Adverse Event
Injury
·ARTA PLAST A-B·Product code FMK·January 31, 2008
HUDSON SOFTECH PLUS ADULT CANNULA,7' GRN STAR-
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAT·September 26, 2021
ANEURX STENT GRAFT
FDA Adverse Event
Death
·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·February 2, 2012
16MM TI END CAP T40 STARDRIVE 5MM EXT-STER/FEMORAL NAILS-EX
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code HSB·February 21, 2013
AIRVANCE¿ THS SYSTEM - TOUNGE SUSPENSION KIT
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code LRK·October 24, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011
LYNX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 1, 2013
SURGICEL ABSORBABLE HEMOSTAT UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code LMG·October 26, 2021
AUVON TENS UNIT
FDA Adverse Event
Injury
·SHEN ZHEN AS TEC TECHNOLOGY CO LTD·Product code NUH·December 19, 2024
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·May 13, 2019
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·May 13, 2019
PIPELINE
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code OUT·April 25, 2018
13.0MM CANNULATED DRILL BIT 300MM
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HWE·August 18, 2017