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

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TELEGRAPH® EVOLUTION Humeral Nailing System

FDA 510(k)
FDA Class 2 ·Orthopedic

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776402853·LANGENBECK RETRACTOR 8.5" 1 5/8" X 1/2" HOLLOW ...

Instrument Tray

FDA UDI
Treace Medical Concepts, Inc.·00810111221795·Instrument Tray

DEBAKEY FORCEPS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896092921·DEBAKEY FORCEPS TUNGSTEN CARBIDE SERRATED TIP F...

Navigator 3 Control Unit

FDA UDI
crystal-photonics GmbH·04260152887102·Gamma Probe System, control unit

7000 CONNECTORS

FDA UDI
HANS RUDOLPH, INC.·00817136022130·CONN 35IDORG X 22OD 7000 SER

Initia Total Hip System

FDA UDI
KYOCERA CORPORATION·04547898306266·STD LINER 32-50

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306823183·Sheehan Osteotome, 7mm, 16cm

Integra® Jarit®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780182108·Integra® Jarit® Langenbeck Retractor, 8-1/2", M...

KURZ PURE GOLD UPPER EYELIDS IMPLANT (OBERASCHER), MODEL 4001 02-4001 10

FDA 510(k)
FDA Class 2 ·Ophthalmic

SMARTFLOW PULSE TRANSMISSION COEFFICIENT

FDA 510(k)
FDA Class 2 ·Cardiovascular

AUVON TENS & EMS DEVICE

FDA Adverse Event
Injury ·SHEN ZHEN AS TEC TECHNOLOGY CO LTD·Product code NUH·January 28, 2025

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962160251·LUNGO PLASTIC TRAY, 13"X9 1/2"X6", W/ SILICONE MAT

VISCOAT OPHTHALMIC VISCOSURGICAL DEVICE

FDA Adverse Event
Injury ·ALCON - COUVREUR N.V./ALCON - BELGIUM·Product code LZP·November 16, 2022

ACRYSOF

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD / HUNTINGTON·Product code HQL·February 15, 2013

SOFTCLIX LANCET DEVICE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·October 15, 2008

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·August 10, 2011

INNOVA?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code FGE·July 1, 2013

AUVON TENS UNIT

FDA Adverse Event
Injury ·SHEN ZHEN AS TEC TECHNOLOGY CO LTD·Product code NUH·December 19, 2024

SINGLE USE GUIDWIRE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code OCY·July 10, 2020