MODIFICATION TO EBI DYNAFIX DIAPHYSEAL CORRECTION SYSTEM

FDA registration

BIOMET, INC.·1 product·🇺🇸 United States

MODIFICATION TO EBI DYNAFIX DIAPHYSEAL CORRECTION SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

MODIFICATION TO SYNTHES CERVIFIX SYSTEM; K030377

FDA registration

EXEL INC. DBA DHL SUPPLY CHAIN (USA)·2 products·🇺🇸 United States

Tornier Latitude

FDA UDI

TORNIER, INC.·00846832020034·SLAPHAMMER ATTACHMENT

everStickPERIO

FDA registration

GC AMERICA INC.·1 product·🇺🇸 United States

everStickPERIO

FDA registration

STICK TECH LTD.·1 product·🇫🇮 Finland

LightLas 532

FDA registration

LIGHTMED CORP.·1 product·🇹🇼 Taiwan

BioniCare Knee

FDA registration

VQ ORTHOCARE·1 product·🇺🇸 United States

Comfort Catheter System

FDA registration

ARGON MEDICAL DEVICES, INC.·1 product·🇺🇸 United States

BioniCare Knee

FDA registration

VQ ORTHOCARE·1 product·🇺🇸 United States

REDLINE ALERT TEST

FDA registration

TETRACORE, INC·1 product·🇺🇸 United States

TriVerse Femoral Component CR

FDA UDI

SIGNATURE ORTHOPAEDICS PTY LTD·09348215100209·

LIGHTLAS 532 PHOTOCOAGULATOR

FDA 510(k)

FDA Class 2 ·Ophthalmic

IMMULITE HIGH SENSITIVITY CRP, IMMULITE 2000 HIGH SENSITIVITY CRP

FDA 510(k)

FDA Class 2 ·Immunology

Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

FDA classification

FDA Class 2 ·Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

System, Test, C-Reactive Protein

FDA classification

FDA Class 2 ·System, Test, C-Reactive Protein

Laser, Ophthalmic

FDA classification

FDA Class 2 ·Laser, Ophthalmic