23 results · 20ms · Sources: EU EUDAMED, US FDA

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MissLan® Early Detection Digital Pregnancy Test; MissLan® Early Result Digital Pregnancy Test

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

LoFric® Hydro-Kit™

FDA UDI
Wellspect AB·07392532148545·Single Use Urinary Catheter LoFric Hydro-Kit Co...

Valence Robotic Navigation System

FDA UDI
ALPHATEC SPINE, INC.·00190376633534·ION Array A

STERILE TRAC SYSTEM

FDA UDI
BIOMET MICROFIXATION, INC·00888233007856·

STERILE TRAC SYSTEM

FDA UDI
BIOMET MICROFIXATION, INC·00841036147709·

FPS

FDA UDI
Tyber Medical, LLC·00810040686238·Ø2.5mm Non-locking Screw, 40mm

IPL HAIR REMOVAL DEVICE CT05

FDA Adverse Event
Injury ·SHENZHEN CHUANGTONG YIGOU TECHNOLOGY CO., LTD.·Product code OHT·February 19, 2026

HAND-HELD HAIR REMOVAL DEVICE

FDA Adverse Event
Injury ·SHENZHEN CHUANGTONG YIGOU TECHNOLOGY CO., LTD.·Product code OHT·March 9, 2026

Preference

FDA UDI
CTL Medical Corporation·00841732153004·7.2mm Triple-lead screw Reduction 40mm Green

STERILE TRAC SYSTEM 12 PACK

FDA UDI
BIOMET MICROFIXATION, INC·00888233007870·

Evolve

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215002671·

STERILE TRAC SYSTEM 12 PACK

FDA UDI
BIOMET MICROFIXATION, INC·00841036131500·

Art-line Single channel blood pressure system, Art-line Double channel blood pressure system, Art-line Triple channel blood pressure system, IAP Monitoring Set with Disposable Transducer

FDA 510(k)
FDA Class 2 ·Cardiovascular

HEPARIN DOSE RESPONSE CONTROLS, MODEL 306-20 POR

FDA 510(k)
FDA Class 2 ·Hematology

Preference 2

FDA UDI
SINTX Technologies, Inc.·M555287251040·ø7.2 Triple Lead Reduction Screw Assembly, 40mm

Vu aPod™ - L

FDA UDI
Seaspine Orthopedics Corporation·10889981046842·LATERAL TRIAL, WIDE, LORDOTIC, 10mm X 23mm X 40...

NA

FDA UDI
aap Implantate AG·04042409194511·Cortical Screw 2.5, self-tapping, L 40

NA

FDA UDI
aap Implantate AG·04042409445347·Cannulated Headless Bone Screw 2.5, L 40, TL 10...

NA

FDA UDI
Exactech, Inc.·10885862523839·TRIAL, TIBIAL BASEPLATE, SIZE 4T

PROLENE POLYPROPYLENE SUTURE

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·November 14, 2014