604 results · 22ms · Sources: EU EUDAMED, 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