78 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.

ALTERA NEBULIZER SYSTEM, MODEL 678G1002

FDA 510(k)
FDA Class 2 ·Anesthesiology

Bur PM2-70 80K diamond coarse Ø3.1mm sterile

FDA UDI
Bien-Air Surgery SA·J00711003800011·

Bur PM2-70 80K Diam C Ø3.1 St

FDA UDI
Bien-Air Surgery SA·17630055503463·

Bleep Dreamway

FDA UDI
BLEEP, LLC·00850003157047·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450238158·

Apex

FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529581060·Apex Femoral Nail PF Left Ø 10.0 x 380mm

Apex

FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529582074·Apex Femoral Nail PF Right Ø 10.0 x 380mm

Mariner MIS

FDA UDI
Seaspine Orthopedics Corporation·10889981214227·MIS Tower Remover

OIC Intramedullary Nail System

FDA UDI
ORTHOPAEDIC IMPLANT COMPANY, THE·M696TIB1003800·TIBIAL NAIL 10MM X 380MM

Apex

FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529586928·Apex Femoral Nail GT Right Ø 10.0 x 380mm

OIC Intramedullary Nail System

FDA UDI
ORTHOPAEDIC IMPLANT COMPANY, THE·M696ARFN1003800·ANTEGRADE RETROGRADE FEMORAL NAIL 10MM X 380MM

OIC Intramedullary Nail System

FDA UDI
ORTHOPAEDIC IMPLANT COMPANY, THE·10811998037476·TIBIAL NAIL 10MM X 380MM

Standard Stainless Steel Braided Archwires

FDA UDI
Ortho Organizers, Inc.·00190707100223·.016 x .016 Upper Stainless Steel Braided Pro F...

OIC Intramedullary Nail System

FDA UDI
ORTHOPAEDIC IMPLANT COMPANY, THE·10811998036639·ANTEGRADE RETROGRADE FEMORAL NAIL 10MM X 380MM

Apex

FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529586027·Apex Femoral Nail GT Left Ø 10.0 x 380mm

Apex

FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529587932·Apex Femoral Nail Retrograde Ø 10.0 x 380mm

SIGN I.M. NAIL

FDA Adverse Event
Injury ·SURGICAL IMPLANT GENERATION NETWORK (SIGN)·Product code HSB·October 24, 2008

FOTOMASTER

FDA 510(k)
FDA Class 2 ·Radiology

MP3HD BIG BOY, POWER WHEELCHAIR

FDA 510(k)
FDA Class 2 ·Physical Medicine

BD SARS-COV-2 REAGENTS FOR BD MAX SYSTEM

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·June 25, 2020