Restore

FDA UDI

KEYSTONE DENTAL, INC.·D768L13003442K0·Drill

SANICURE BV

FDA registration

SANICURE BV·1 product·🇳🇱 Netherlands

Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

FDA classification

FDA Class 2 ·Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

GENESYS SPINE INTERBODY FUSION SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

RADIOGRAPHIC X-RAY SYSTEM

FDA 510(k)

FDA Class 2 ·Radiology

COOPDECH ENDOBRONCHIAL BLOCKER TUBE, MODELS BBT-A30XXX, BBT-B30XXX

FDA 510(k)

FDA Class 2 ·Anesthesiology

SUPERCATH 5

FDA 510(k)

FDA Class 2 ·General Hospital

CRYSTALEYE SPECTROPHOTOMETER/CRYSTALEYE BASIC SET, MODEL CE100-DC/US

FDA 510(k)

FDA Class 2 ·Dental

SUPERCATH V

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

MODIFICATION TO DBB-05 HEMODIALYSIS DELIVERY SYSTEM

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

NIKKLINE BLOOD TUBING LINES WITH TRANSDUCER PROTECTORS, MODELS AV06A-P, AVO6B-P, AV06C-P

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

SPIRO-MASTER PC-10 SPIROMETRY SYSTEM

FDA 510(k)

FDA Class 2 ·Anesthesiology

System, X-Ray, Stationary

FDA classification

FDA Class 2 ·System, X-Ray, Stationary

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar