278 results · 22ms · Sources: EU EUDAMED, US FDA

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LEGACY® IPC

FDA 510(k)
FDA Class 2 ·Cardiovascular

NA

FDA UDI
SYNTHES (U.S.A.) LP·10886982159694·3.5MM 90 DEG CANN LC-ANGLED BLADE PLATE 10 HOLE...

MEGA PLUS SPINE SYSTEM

FDA UDI
BK MEDITECH CO.,LTD.·08809665580344·Rod(CoCr), Ø5.5 x 60mm

Introcan Safety ® 2

FDA UDI
B. BRAUN MEDICAL INC.·04046955341894·Introcan Safety 2 - 20G x 1.0 in., PUR, Straight

OsteoMed

FDA UDI
OSTEOMED LLC·00845694017961·MFx 2.0mm x 6mm Angulated Locking Auto-Drive Screw

ENT Plasma Wands, Turbinator Wand, Werewolf Irrigation Tube Set, Werewolf ENT Adapter, Werewolf Coblation System

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

STERILE NITRILE POWDER FREE EXAMINATION GLOVE(VBLU), STERLE NITRILE POWDER FREE EXAMINATION GLOVE(ABLU)

FDA 510(k)
FDA Class 1 ·General Hospital

Cable-Ready®

FDA UDI
Zimmer, Inc.·00889024039544·

HAMILTON MEDICAL AG

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·May 2, 2023

HAMILTON-C6

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·May 12, 2024

HAMILTON MEDICAL AG

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·March 28, 2023

HAMILTON-C3

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·January 16, 2024

HAMILTON-C3

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·February 13, 2024

QUICK CONNECT DRILL

FDA Adverse Event
Malfunction ·BIOMET, INC.·Product code HTW·March 8, 2006

NEXGEN COMPLETE KNEE SOLUTION LEGACY KNEE-POSTERIOR

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JWH·April 21, 2006

HAMILTON-C6

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·April 7, 2026

INSIGNIA ULTRA

FDA Adverse Event
Death ·Product code DXY·July 27, 2007

KENTROX SL-S 65/16

FDA Adverse Event
Other ·BIOTRONIK GMBH AND CO.·Product code DTB·March 2, 2006

ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GCJ·August 23, 2006

ULTRA SONIC CLEANER

FDA Adverse Event
Malfunction ·STERIS CORPORATION·Product code FLG·August 22, 2006