19 results · 20ms · Sources: EU EUDAMED, US FDA

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Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)

FDA 510(k)
FDA Class 2 ·Dental

Darby Dental Supply, LLC

FDA UDI
DARBY DENTAL SUPPLY, LLC·00889813053287·NITI ROTARY FILE S20/T06 31MM DARBY

ELMED

FDA UDI
ELMED INCORPORATED·00842180182837·5MM DIA., 35CM, ESOPHAGEAL - LAP BANDING RETRAC...

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776151676·ESOPHAGEAL LAP BAND MANIPULATOR WITH ROUND HAND...

Portex

FDA UDI
ICU MEDICAL, INC.·10351688429735·

INTUITION

FDA UDI
DEPUY (IRELAND)·10603295544586·INTUITION FOR HP PARTIAL FEMORAL FINISHING BLOC...

INTUITION

FDA UDI
DEPUY (IRELAND)·10603295544609·INTUITION FOR HP PARTIAL FEMORAL FINISHING BLOC...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197177009·Watson-Williams Ethmoidal Forceps Fig. 2 WL 115...

INTUITION

FDA UDI
DEPUY (IRELAND)·10603295544548·INTUITION FOR HP PARTIAL FEMORAL FINISHING BLOC...

INTUITION

FDA UDI
DEPUY (IRELAND)·10603295544562·INTUITION FOR HP PARTIAL FEMORAL FINISHING BLOC...

INTUITION

FDA UDI
DEPUY (IRELAND)·10603295544623·INTUITION FOR HP PARTIAL FEMORAL FINISHING BLOC...

INTUITION

FDA UDI
DEPUY (IRELAND)·10603295544524·INTUITION FOR HP PARTIAL FEMORAL FINISHING BLOC...

FU HONG INDUSTRIES LIMITED SOOTHER TEETHER

FDA 510(k)
FDA Class 2 ·Dental

InstaClear Lens Cleaner

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 15, 2014

IVT DISPOSABLE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MALTA·Product code KPE·September 17, 2011

GYNECARE TVT-AA ABDOMINAL

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTN·July 29, 2013

Exactech Equinoxe REVERSE SHOULDER,42mm Humeral Liner, a) +0mm, Item number 320-42-00, b) +2.5mm, Item Number 320-42-03; Shoulder Arthroplasty

FDA Enforcement
Class II ·Ongoing·Exactech, Inc.·April 10, 2024

Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020

FDA Enforcement
Class II ·Terminated·Cardinal Health 200, LLC·February 26, 2020