120 results · 25ms · 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.

TYRX Neuro Absorbable Antibacterial Envelope (medium); TYRX Neuro Absorbable Antibacterial Envelope (large)

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

Maestro™ Total Wrist

FDA UDI
Biomet Orthopedics, LLC·00887868239496·

MAESTRO TOTAL WRIST

FDA UDI
Biomet Orthopedics, LLC·00880304439122·

Novo Surgical

FDA UDI
NOVO SURGICAL, INC.·G586G1801220·peet splinter forceps, angled, 4 1/2" (11.5 cm)

Super Upper Limbs Versalock Plating System

FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258663609·VERSALOCK SPANNING PLATE 115.0mm, SEMI ANGLED

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361011545·PedFuse Respond, CNL, 6.0mm x 55mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361011491·PedFuse Respond, CNL, 6.0mm x 30mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361011521·PedFuse Respond, CNL, 6.0mm x 45mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361011514·PedFuse Respond, CNL, 6.0mm x 40mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361011507·PedFuse Respond, CNL, 6.0mm x 35mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361011538·PedFuse Respond, CNL, 6.0mm x 50mm

TWIST DRILL

FDA UDI
Biomet Orthopedics, LLC·00887868017636·

DePuy Mitek

FDA UDI
Provision·B504OM1801220000·

MODIFICATION TO CAPSURE PS SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

SOPRO 670 ARTHROSCOPIC PUMP

FDA 510(k)
FDA Class 2 ·Orthopedic

NA

FDA UDI
STERILMED, INC.·10888551009461·DRILL BIT TWIST

MUSTANG?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 25, 2025

MUSTANG?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·April 22, 2025

MUSTANG?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LIT·April 28, 2025

MUSTANG?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·August 18, 2025