604 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0112420·Awl Tap, 4.75 mm, Fixed Sleeve
HUANQIU AND SUPER (TWO BRANDS) STERILE ACUPUNCTURE NEEDLE FOR SINGLE USE
FDA 510(k)
FDA Class 2
·General Hospital
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040015186·Zirlux 16+ A3.5 85x40x22
ODYSSEY®
FDA UDI
Microport Orthopedics Inc.·M684K00112421·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0112020·Tap, 4.75mm
ISOLETTE INFANT INCUBATOR, MODEL C2HS
FDA 510(k)
FDA Class 2
·General Hospital
COOK ZILVER BILIARY STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
IMPL TAPERED SP 3.7MM 10M M OCTAGON
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·February 25, 2022
IMPL TAPERED SP 3.7MM 8MM OCTAGON
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·January 13, 2022
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTN·March 19, 2013
MINI-CAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·March 8, 2011
BARDEX ALL-SILICONE FOLEY CATHETER
FDA Adverse Event
BARD UROLOGICAL DIVISION·Product code KOD·February 26, 2008
IMPL TAPERED SP 3.7MM 14M M OCTAGON
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·October 14, 2022
IMPL TAPERED SP 4.8MM 8MM OCTAGON
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·November 17, 2022
IMP AV SBM 3.7MM 4.5MM IN TERFACE 10MM
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·March 26, 2026
IMPL TAPERED SP 3.7MM 10M M OCTAGON
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·January 8, 2021
IMPL TAPERED SP 4.8MM 14M M OCTAGON
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·January 21, 2022
IMP AV SBM 3.7MM 4.5MM IN TERFACE 16MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·October 14, 2022
IMPL TAPERED SP 4.8MM 8MM OCTAGON
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·February 24, 2020
MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142515, K153343, K173592, K202014, K231560.
FDA Recall
Open, Classified
·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025