29 results · 21ms · Sources: EU EUDAMED, US FDA

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HARDYDISK, CEFAZOLIN, 30MCG

FDA 510(k)
FDA Class 2 ·Microbiology

Deployment Skid Cannula Access Tool

FDA UDI
Anika Therapeutics, Inc.·00817337000319·Reusable non-rigid cannula access tool

PowerPICC

FDA UDI
Bard Access Systems, Inc.·00801741042584·Catheter Placement Kit

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00012881·

TruFlex™

FDA UDI
Ortho Organizers, Inc.·00190707127299·Truflex™ PT SE NiTi Upper 17x25 34mm (10PK)

TruFlex

FDA UDI
ORTHO TECHNOLOGY, INC.·00190730011848·Truflex™ PT SE NiTi Upper 17x25 34mm 10/PK

CURE™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167700001280·

CURE 2.0 ACP

FDA UDI
SpineArt SA·07640375232328·ANTERIOR CERVICAL PLATE, 1 LEVEL L28

CURE™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167S1700001280·

CURE 2.0 ACP

FDA UDI
SpineArt SA·07640375230935·CERVICAL 1 LEVEL TEMPLATE L28

RENAFLO II HF 2000 HEMOFILTER

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

RAPID RHINO-ANTERIOR 90MM, MODEL RR-A 90, RAPID RHINO-POSTERIOR 100MM, MODEL RR-P 100

FDA 510(k)
FDA Class 1 ·Ear, Nose, Throat

SMR REVERSE HUMERAL BODY

FDA Adverse Event
Injury ·LIMACORPORATE S.P.A.·Product code KWS·October 21, 2022

NIROYAL BILIARY STENT

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION, IRELAND, LTD.·Product code FGE·July 31, 2002

ULTRA-THIN BALLOON DILATATION CATHETER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION, IRELAND, LTD.·Product code LIT·July 31, 2002

WALLACH ULTRA FREEZE

FDA Adverse Event
Malfunction ·COOPERSURGICAL, INC.·Product code GEH·July 11, 2023

LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 9.75CM

FDA Adverse Event
Malfunction ·ALLERGAN·Product code LTI·February 14, 2013

POWER PRO AMBULANCE COT

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code INK·February 3, 2011

LUGE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC·Product code DQX·February 19, 2008

ADVANTA V12,COVERED STENTSYS,10X59X120

FDA Adverse Event
Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·December 10, 2025