1,655 results · 23ms · Sources: EU EUDAMED, US FDA

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FLUID FILLED TEETHER - GEL

FDA 510(k)
FDA Class 2 ·Dental

DELTA

FDA UDI
Stryker Leibinger GmbH & Co. KG·07613252616108·DELTA 1.7MM DOUBLE Y-PLATE 8 HOLE, 0.5MM

Instrument Case

FDA UDI
KATENA PRODUCTS, INC.·00841668110973·STERILIZING CASE MEDIUM/SMALL

Vilex Power Accessory

FDA UDI
VILEX IN TENNESSEE, INC.·00841731122193·KWire .035x9" (0.9x225mm)

Titan™

FDA UDI
Ascension Orthopedics, Inc.·10381780243236·Titan™ Total Shoulder System The Titan Modular ...

RIGID GAS PERMEABLE CONTACT LENS

FDA 510(k)
FDA Class 2 ·Ophthalmic

MACROPORE SURGIWRAP (TS)

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

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 10, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 11, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 11, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

CD HORIZON® SPINAL SYSTEM

FDA Adverse Event
Death ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 4, 2017

MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·September 30, 2025

PUMP MMT-1885A OUS BLE PUMP MMOL/L

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 11, 2025

CELL-DYN RUBY

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code GKZ·September 16, 2025

PUMP MMT-1880L MM770G BLE MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·September 30, 2025