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

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Turbett Surgical Container

FDA 510(k)
FDA Class 2 ·General Hospital

LEONE SPA

FDA UDI
LEONE SPA·08033707014799·CALIBRA 1ST MOL BANDS W/G8325-03 n.UL 25

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100288·SAUER PREMATURE INFANT SPECULUM 2MM

MORRISON MEDICAL

FDA UDI
MORRISON MEDICAL, LTD·00647921153028·CDBD.SPLINT,18"CTR. FOAM,CS/25

BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·May 9, 2024

Truliant

FDA UDI
Exactech, Inc.·10885862523402·PS NOTCH CUTTER, SIZE 2.5

GIVEN PILLCAM PLATFORM WITH RAPID 6.5 / GIVEN PILLCAM PLATFORM WITH PILLCAM ESO 3 CAPSULES

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

JOSTRA HLM TUBING SET

FDA 510(k)
FDA Class 2 ·Cardiovascular

IHEARTEST

FDA Adverse Event
Malfunction ·IHEAR MEDICAL, INC.·Product code EWO·August 17, 2022

BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·May 14, 2024

BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·February 29, 2024

BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·May 14, 2024

U BY KOTEX CLICK : TAMPON, MENSTRUAL, UNSCENTED : HEB

FDA Adverse Event
Malfunction ·QINGDAO P&B CO., LTD.·Product code HEB·October 8, 2014

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code DTB·June 8, 2013

HEARTSTART FRX

FDA Adverse Event
Death ·PHILIPS MEDICAL SYSTEMS (HTST)·Product code MKJ·June 28, 2011

ELEKTA LIMITED Versa HD, REF XRT 2121, 2131; Medical Charged-Particle Radiation Therapy System Accelerator, Linear

FDA Enforcement
Class II ·Ongoing·Elekta, Inc.·December 13, 2023