25 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CryoTreQ
FDA 510(k)
FDA Class 2
·Ophthalmic
Conventional Lead Apron .5mm Xtra Large 25 X 40
FDA UDI
Flow X Ray Corporation·00843696123727·Conventional Lead Apron .5mm Xtra Large 25 X 40...
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112519·BARRON VACUUM TREPHINE 8.0MM
SprintRay High Impact Denture Base - Light Pink
FDA UDI
Sprintray, Inc.·00850039704185·SprintRay High Impact Denture Base is a light-c...
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112632·BARRON CORNEAL PUNCH 8.0MM
SPI ONETIME DENTAL IMPLANT
FDA 510(k)
FDA Class 2
·Dental
Endosee System
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ACCU-CHEK ® GUIDE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIABETES CARE, INC.·Product code NBW·August 14, 2020
ACCU-CHEK GUIDE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIABETES CARE, INC.·Product code NBW·August 14, 2020
Trabecular Metal®
FDA UDI
Zimmer, Inc.·00889024118652·
Trabecular Metal®
FDA UDI
Zimmer, Inc.·00889024118669·
Trabecular Metal®
FDA UDI
Zimmer, Inc.·00889024118676·
LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (STANDARD)
FDA Adverse Event
Injury
·ALLERGAN·Product code LTI·August 5, 2011
PENTA
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 21, 2014
GYNECARE PROLIFT ANTERIOR PELVIC FLOOR REPAIR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·July 2, 2013
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·June 21, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·July 5, 2022
CHAIT PERCUTANEOUS CECOSTOMY CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KNT·June 10, 2025
PER-Q-CATH PLUS 4F SINGLE-LUMEN PICC WITH SAFETY EXCALIBUR INTRODUCER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·February 26, 2021
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·April 12, 2023