129 results · 23ms · Sources: EU EUDAMED, US FDA

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Neodent Implant System-Easy Pack

FDA 510(k)
FDA Class 2 ·Dental

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113400·IMPLANT KNIFE 4.0MM (BX/5)

Ophthalmic Cannula

FDA UDI
KATENA PRODUCTS, INC.·00841668114094·SIMCOE CORTEX EXTRACTOR 23GA 0.4MM PK/10

SARSTEDT NEEDLE PROTECTOR

FDA 510(k)
FDA Class 2 ·General Hospital

COOPERSURGICAL MALLEABLE SYTLET

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

MUST LT 25MM LONG - PEDICLE SCREW Ø6X45 CANN

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·January 19, 2024

MUST LT 03.57.035 MUST LT 15MM SHORT - PEDICLE SCREW Ø7X45 CANN

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 18, 2022

M.U.S.T. PEDICLE SCREW SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·September 18, 2025

PEDICLE SCREW MUST LT 15MM SHORT - PEDICLE SCREW Ø4.5X30 CANN

FDA Adverse Event
Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·November 8, 2023

M.U.S.T. PEDICLE SCREW SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·July 16, 2025

MUST LT 03.59.234 MUST LT 25MM LONG - PEDICLE SCREW Ø7X40 CANN

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·February 16, 2022

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 27, 2014

ATTAIN OTW

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

GYNECARE TVT OBURATOR SYSTEM

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTN·July 2, 2013

MUST LT 15MM SHORT - PEDICLE SCREW Ø8X40 CANN

FDA Adverse Event
Death ·MEDACTA INTERNATIONAL SA·Product code NKB·March 29, 2023

AVID TruCustom PLASTIC BASIN PACK convenience kits, Item Code: MADN008-03

FDA Enforcement
Class II ·Terminated·Avid Medical, Inc.·March 7, 2018

HF UNIT "ESG-400"

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GEI·November 19, 2023

ELECTROSURGICAL GENERATOR "ESG-400"

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GEI·July 8, 2022

ELECTROSURGICAL GENERATOR "ESG-400"

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GEI·October 18, 2022

ELECTROSURGICAL GENERATOR "ESG-400"

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GEI·October 24, 2022