25 results · 21ms · Sources: EU EUDAMED, US FDA

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AtriCure cryoICE cryo-ablation probe (CRYO3), AtriCure cryoICE cryoFORM cryo-ablation probe (CRYOF)

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

PedFuse

FDA UDI
SPINEFRONTIER, INC.·00190361034148·PedFuse Remind LES, Quad-H, 6.0mm x 30mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012917·PedFuse Remind LES, Quad-H, 6.0mm x 45mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012900·PedFuse Remind LES, Quad-H, RBM Coated, 6.0mm x...

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012931·PedFuse Remind LES, Quad-H, 6.0mm x 50mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012887·PedFuse Remind LES, Quad-H, RBM Coated, 6.0mm x...

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012962·PedFuse Remind LES, Quad-H, RBM Coated, 6.0mm x...

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012948·PedFuse Remind LES, Quad-H, RBM Coated, 6.0mm x...

PedFuse

FDA UDI
SPINEFRONTIER, INC.·00190361034155·PedFuse Remind LES, Quad-H, RBM Coated, 6.0mm x...

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012955·PedFuse Remind LES, Quad-H, 6.0mm x 55mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012870·PedFuse Remind LES, Quad-H, 6.0mm x 35mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012924·PedFuse Remind LES, Quad-H, RBM Coated, 6.0mm x...

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012894·PedFuse Remind LES, Quad-H, 6.0mm x 40mm

Super Upper Limbs Versalock Plating System

FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258663371·VERSALOCK VOLAR DOUBLE ROW PLATE 22.0x34.0mm, LEFT

Super Upper Limbs Versalock Plating System

FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258663364·

ONE TOUCH ULTRA

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CFR·June 30, 2003

ABX PENTRA ENZYMATIC CREATININE CP, ABX PENTRA MULTICAL, ABX PENTRA N CONTROL, ABX PENTRA P CONTROL, AND ABX PENTRA URIN

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

SIDEKICK CIRCULAR FIXATOR SYSTEM: STRUTS AND HINGES

FDA 510(k)
FDA Class 2 ·Orthopedic

COMP RVS CNTRL SCR 6.5X30MM ST

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWS·October 17, 2014

SITTER SELECT

FDA Adverse Event
Malfunction ·J. T. POSEY CO.·Product code KMI·June 4, 2013