661 results · 72ms · Sources: EU EUDAMED, US FDA

Bioretec Ltd.

Manufacturer
🇫🇮 Finland·287 Basic UDI-DIs·346 Devices·DEKRA Certification B.V., DEKRA Certification B.V., DEKRA Certification B.V., and DEKRA Certification B.V.

Activa Instruments

FDA registration
Bioretec Ltd.·1 product·🇫🇮 Finland

ActivaNail Conical

FDA registration
Bioretec Ltd.·1 product·🇫🇮 Finland

ActivaScrew Cannulated

FDA registration
Bioretec Ltd.·1 product·🇫🇮 Finland

RemeOs Screw LAG Solid

FDA registration
Bioretec Ltd.·1 product·🇫🇮 Finland

RemeOs Instrument

FDA registration
Bioretec Ltd.·1 product·🇫🇮 Finland

ActivaScrew Interference

FDA registration
Bioretec Ltd.·1 product·🇫🇮 Finland

ActivaPinTM

FDA registration
Bioretec Ltd.·1 product·🇫🇮 Finland

Activa

FDA registration
Bioretec Ltd.·1 product·🇫🇮 Finland

ACTIVAPIN, NEXFIX RFS PIN, NEXFIX RESORBABLE FIXATION SYSTEM (RFS)

FDA 510(k)
FDA Class 2 ·Orthopedic

ACTIVAPIN HT, FUSE LINK (PRIVATE LABLED FOR FOOTMIND, INC.)

FDA 510(k)
FDA Class 2 ·Orthopedic

ACTIVATM PRODUCT GROUP INCLUDING BIOABSORBABLE DEVICES ACTIVAPIN FUSION, ACTIVANAILTM CONICALTM

FDA 510(k)
FDA Class 2 ·Orthopedic

ACTIVASCREW

FDA 510(k)
FDA Class 2 ·Orthopedic

BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN

FDA 510(k)
FDA Class 2 ·Orthopedic

RemeOs™ Screw LAG Solid

FDA 510(k)
FDA Class 2 ·Orthopedic

BIORETEC ACTIVASCREW INTERFERENCE

FDA 510(k)
FDA Class 2 ·Orthopedic

ACTIVAPIN

FDA 510(k)
FDA Class 2 ·Orthopedic

ACTIVASCREW

FDA 510(k)
FDA Class 2 ·Orthopedic

Applicator Ø3.2 mm, reusable, for 3.2 mm pins and for 1.5/2.0/2.7/3.2 mm nails

Device
EU MDR · Eu Md Class 1 ·Bioretec Ltd.·On the market·32 countries

Applicator Ø2.7 mm, reusable, for 2.7 mm pins

Device
EU MDR · Eu Md Class 1 ·Bioretec Ltd.·On the market·32 countries