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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Occluder, Patent Ductus, Arteriosus

FDA Pre-Market Approval
FDA Class 3 ·NIT-OCCLUD PDA

Occluder, Patent Ductus, Arteriosus

FDA Pre-Market Approval
FDA Class 3 ·NIT-OCCLUD PDA

Occluder, Patent Ductus, Arteriosus

FDA Pre-Market Approval
FDA Class 3 ·PMA NIT-OCCLUD PDA

Occluder, Patent Ductus, Arteriosus

FDA Pre-Market Approval
FDA Class 3 ·NIT-OCCLUD PDA

Occluder, Patent Ductus, Arteriosus

FDA Pre-Market Approval
FDA Class 3 ·NIT-OCCLUD SYSTEM

MIRABAY

FDA UDI
Mirabay Orthodontics Corp.·05061075023146·KLEOS 2 PSL METAL HIGH TORQUE 022 LL12-LR12 PK5...

DURAVENT

FDA UDI
Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948006674·DURAVENT XL, SIZE 9

EVOS Lumbar Interbody System

FDA UDI
Cutting Edge Spine, LLC·00841193109886·HA PEEK EVOS Straight, ,9mmx8mmx 22mm , BICONVE...

PATIENT CIRCUITS

FDA UDI
Zoll Medical Corporation·00847946023140·MASK, CPAP, #4, CHILD

Ventlab

FDA UDI
VENTLAB, LLC·30889483271067·PVC Anesthesia Mask #4, Adult - M, 100/CA

PATIENT CIRCUITS

FDA UDI
Zoll Medical Corporation·10847946023147·MASK, CPAP, #4, CHILD

TESTOSTERONE TEST SYSTEM; CALIBRATOR; AND QUALITY CONTROL MATERIAL (ASSAYED AND UNASSAYED)

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

MOBI-C IMPLANT M "STANDARD" 15X17 H4.5

FDA Adverse Event
Injury ·LDR MEDICAL·Product code MJO·April 22, 2020

PREMICRON GREEN 3/0 (2) 17X45CM

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAT·April 7, 2022

MOBI-C P&F IMPLANT 19X19 H05

FDA Adverse Event
Injury ·LDR MEDICAL·Product code MJO·February 4, 2020

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·EXPRESS/EXPRESS 2 MR & OTW CORONARY STENT SYSTEMS

Mitral Valve Repair Devices

FDA Pre-Market Approval
FDA Class 3 ·MITRACLIP DELIVERY SYSTEM

OBTRYX SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 20, 2013

SECURE II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·May 26, 2011

MICROSTAAR INJECTOR CARTRIDGE

FDA Adverse Event
Malfunction ·STAAR SURGICAL COMPANY·Product code KYB·August 14, 2008