22 results · 42ms · Sources: EU EUDAMED, US FDA

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APD LUER-LOCK ADAPTER

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

MAX-TI HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304225268·

CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 24mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665033557·

Diversatek Healthcare

FDA UDI
DIVERSATEK HEALTHCARE, INC.·M7831240240·Straight Thoracic Catheter, 24 French x 20 IN

Alltest Multi-Drug 13 Drugs Rapid Urine Test Panel

FDA UDI
Hangzhou AllTest Biotech Co., Ltd.·16936983179642·25T, FDA CLIA WAIVED, white package, MOP(OPI)30...

MiniSPC Button

FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071152369·12F x 4.0cm MiniSPC Low Profile Suprapubic Cath...

Segmental Plating System

FDA UDI
ALPHATEC SPINE, INC.·00190376545752·SPS VA Self-Drill Screw, 4.0 x 24mm

Atoll™

FDA UDI
Seaspine Orthopedics Corporation·10889981052553·4.0mm x 24mm Poly Screw Assm. The Atoll OCT Spi...

Sochi

FDA UDI
Altus Spine, LLC·00843210166667·Polyaxial Screw, 4.0mm x 24mm

Insignia

FDA UDI
ALPHATEC SPINE, INC.·00190376329994·4.0mm Variable Angle, Self-Drilling Screw, Sing...

Proximity

FDA UDI
ALPHATEC SPINE, INC.·00190376694863·PROXIMITY VA SELF-DRILL SCREW, 4.0 x 24mm

MECTALIF TRANSFORAMINAL

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDSOURCE IV ADMINSTRATION SET

FDA 510(k)
FDA Class 2 ·General Hospital

MECTALIF ANTERIOR STAND-ALONE PLATE FLUSH H.12 MM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·March 29, 2018

CN LOCK SCREW, F THREAD, Ø4.0MM X 24MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code KTW·June 12, 2024

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Injury ·ANIMAS CORPORATION·Product code LZG·May 22, 2013

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 27, 2014

MAXIMO VR

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code LWS·June 14, 2011

SPECTRA WAVEWRITER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 10, 2019

ALIF SCREWDRIVER UNIVERSAL JOINT

FDA Adverse Event
Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·January 15, 2016