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

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Wedge Microcatheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

BRUSIO 2.5mm Flex Straight Plate, 14 Hole

FDA UDI
Bonebridge AG·07640187463248·

OsteoMed

FDA UDI
OSTEOMED LLC·00845694027007·2.0mm X 14mm Cannulated Headless Screw

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613085087·Sideport Knife, Angled, 1.4mm, 6 Per Box

LVIS Jr.

FDA UDI
Microvention, Inc.·00842429100806·Stent

LVIS Jr.

FDA UDI
Microvention, Inc.·00810170018978·Stent

LVIS Jr.

FDA UDI
Microvention, Inc.·00812636020136·Stent

HORICO

FDA UDI
Hopf, Ringleb & Co. GmbH & Cie.·EHORFG1720142·Rotary Diamond Instrument

HORICO

FDA UDI
Hopf, Ringleb & Co. GmbH & Cie.·EHORFG1720145·Rotary diamond instrument

VITASCORE

FDA 510(k)
FDA Class 2 ·Anesthesiology

TENS STIMULATOR, MODELS 2800 AND 3000

FDA 510(k)
FDA Class 2 ·Neurology

OsteoMed

FDA UDI
OSTEOMED LLC·00845694068444·Cannulated 2.0 x 14mm Headless Screw Sterile Qty 5

PUSHING CATHETER

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·October 19, 2022

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013

INFUSOMAT SPACE

FDA Adverse Event
Malfunction ·B. BRAUN·Product code FRN·July 12, 2011

ABBOTT VASCULAR

FDA Adverse Event
Injury ·ABBOTT LABS·Product code DQX·September 23, 2008

ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020

ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020

FILIFORM DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·June 30, 2022

PUSHING CATHETER

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·September 15, 2023