247 results · 20ms · Sources: EU EUDAMED, US FDA

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Ultrasound Scanner System BK2300

FDA 510(k)
FDA Class 2 ·Radiology

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100264·KATENA DBL-X ASPIRATING SPECULUM K-WIRE

CASTROVIEJO NEEDLE HOLDER

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896017689·CASTROVIEJO NEEDLE HOLDER WITH LOCK CURVED TUNG...

KOMET Surgical Saw Blade

FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613274729·

KOMET Surgical Saw Blade

FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613274620·

KOMET Surgical Saw Blade

FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613064306·

KOMET Surgical Saw Blade

FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613049853·

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575294749·Knee tibia prosthesis trial, reusable - Endo Mo...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575294725·Knee tibia prosthesis trial, reusable - Endo Mo...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575294763·Knee tibia prosthesis trial, reusable - Endo Mo...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575294701·Knee tibia prosthesis trial, reusable - Endo Mo...

MAXISONIC FAMILY AND SWIFT ULTRASONIC SCALER

FDA 510(k)
FDA Class 2 ·Dental

3M ATTEST RAPID READOUT STEAM PROCESS CHALLENGE DEVICE, MODEL 1296V, 3M ATTEST RAPID READOUT STEAM-PLUS

FDA 510(k)
FDA Class 2 ·General Hospital

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 10, 2025

INFUSOMAT®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 11, 2025

CARELINK

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code KRG·June 7, 2013

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Injury ·ANIMAS CORPORATION·Product code LZG·July 7, 2011

LAMITRODE 88

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 6, 2014

INFUSOMAT®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 11, 2026

INFUSOMAT®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 7, 2026