273 results · 36ms · 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.

SOL-M Syringe

FDA UDI
Sol-Millennium Medical, Inc.·00818392018219·SOL-M 10ml Luer Lock Syringe w/o Needle

Stent, Carotid

FDA Pre-Market Approval
FDA Class 3 ·Gore Carotid Stent

Stent, Carotid

FDA Pre-Market Approval
FDA Class 3 ·GORE Carotid Stent

Stent, Carotid

FDA Pre-Market Approval
FDA Class 3 ·GORE Carotid Stent

Stent, Carotid

FDA Pre-Market Approval
FDA Class 3 ·GORE Carotid Stent

Pro Advantage

FDA UDI
NATIONAL DISTRIBUTION & CONTRACTING, INC.·M220P0800103·Pro Advantage Urinalysis Reagent Strips 10 Para...

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361008361·PedFuse Respond, CNL, 5.0mm x 40mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361008330·Pedicle Screw Assy. 5mm Respond

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361008385·PedFuse Respond, CNL, 5.0mm x 50mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361008323·Pedicle Screw Assy. 5mm Respond

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361008354·PedFuse Respond, CNL, 5.0mm x 35mm

Sorrento Bioglass 10cc (100 x 20 x 5 mm)

FDA UDI
XENCO MEDICAL LLC·B064HB1180010·

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361008347·PedFuse Respond, CNL, 5.0mm x 30mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361008378·PedFuse Respond, CNL, 5.0mm x 45mm

Batrik Arc Wire Brushes Single Use

FDA UDI
Batrik Medical Manufacturing Inc·00690521008960·Brush/Red/BD 10mm/BL 50mm/OL 75cm - Rigid - SIN...

AtriClip FLEX-V

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

Free-Lock®

FDA UDI
Zimmer, Inc.·00889024035331·

TECNIS

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code MFK·June 24, 2014

GREENLIGHT MOXY FIBER OPTIC

FDA Adverse Event
Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·October 17, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011