38 results · 39ms · Sources: EU EUDAMED, US FDA

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Pencylcap

FDA 510(k)
FDA Class 2 ·General Hospital

Permacol

FDA UDI
SOFRADIM PRODUCTION·10884523000221·Surgical Implant

Epredia

FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693063753·The blades and knifes consumables are for use w...

TiMesh

FDA UDI
MEDTRONIC PS MEDICAL, INC.·00643169620407·ISOGRID 015-2050 STANDARD 75MM X 75MM

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B16741520500·

TiMesh®

FDA UDI
MEDTRONIC PS MEDICAL, INC.·00673978003214·ISOGRID 015-2050 STANDARD 75MM X 75MM

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100158·KRATZ-BARRAQUER SPECULUM LARGE

MORRISON MEDICAL

FDA UDI
MORRISON MEDICAL, LTD·00647921152052·PLAIN CARDBD SPLINT 24", CA 50

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B1674152050060·

Q-SWITCHED ND:YAG LASER SYSTEM, MODEL GLOBALCURE-SC6

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

SOUNDSTAR ECO DIAGNOSTIC ULTRASOUND CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

NA

FDA UDI
Zimmer, Inc.·00889024033955·

Truliant

FDA UDI
Exactech, Inc.·10885862523341·PS NOTCH GUIDE, SIZE 5

TENDRIL STS

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code DTB·January 13, 2014

BIORAPTOR AB 2.9 MM

FDA Adverse Event
Malfunction ·SMITH & NEPHEW ENDOSCOPY·Product code HWC·July 7, 2011

CARELINK

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

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 30, 2022

KYPHON BONE CEMENT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·April 23, 2019

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·March 18, 2026

METACROSS OTW PTA BALLOON DILATATION CATHETER

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2019