10,000 results · 63ms · Sources: EU EUDAMED, US FDA

Unit, Oral Irrigation - ETEKCITY Water Flosser, EWF-32

FDA registration
VESYNC (SINGAPORE) PTE.LTD.·1 product·🇸🇬 Singapore

Importer:Atomic

FDA registration
KEY-JOINT INDUSTRIES INC.·1 product·🇹🇼 Taiwan

Electric laser hair generator( Aurora-650)

FDA registration
ADVANTEK OPTOELECTRONICS TECHNOLOGY (CHANGZHOU) CO., LTD·1 product·🇨🇳 China

Isolation Eyes Cover

FDA registration
ADVANTEK OPTOELECTRONICS TECHNOLOGY (CHANGZHOU) CO., LTD·1 product·🇨🇳 China

LED Mask(LED YM 5W)

FDA registration
ADVANTEK OPTOELECTRONICS TECHNOLOGY (CHANGZHOU) CO., LTD·1 product·🇨🇳 China

0.6T Panorama 4Ch Breast Array

FDA registration
Philips Global Business Services LLP·1 product·🇮🇳 India

0.6T Panorama 4Ch Breast Array

FDA registration
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·1 product·🇳🇱 Netherlands

0.6T Panorama 4Ch Breast Array

FDA registration
Philips Electronics Ltd·1 product·🇨🇦 Canada

GUANG ZHOU TIAN SI PIN HUI INDUSTRIAL CO., LTD

Manufacturer
🇨🇳 China

Prosthetic Accessories

FDA UDI
A.B. DENTAL DEVICES LTD·07290107271592·Narrow Titanium Healing Cap

Prosthetic Accessories

FDA UDI
A.B. DENTAL DEVICES LTD·07290107271622·Narrow Titanium Healing Cap

Prosthetic Accessories

FDA UDI
A.B. DENTAL DEVICES LTD·07290107271608·Narrow Titanium Healing Cap

Prosthetic Accessories

FDA UDI
A.B. DENTAL DEVICES LTD·07290107271585·Narrow Titanium Healing Cap

Healing Cap

FDA registration
S.G.S. INTERNATIONAL LTD·2 products·🇭🇺 Hungary

SHANGHAI PLATINUM PEN CO., LTD.

FDA registration
SHANGHAI PLATINUM PEN CO., LTD.·1 product·🇨🇳 China

RESIN CEMENT POWDER

FDA UDI
AMERICAN TOOTH INDUSTRIES·D772ATI800400NY0·RESIN CEMENT POWDER 1/2 OZ N. YELLOW

STERILUX BULKY GZ N-ST 4.5X4.1 100/CS

FDA UDI
HARTMANN USA, INC.·10612553024807·STERILUX BULKY GZ N-ST 4.5X4.1 100/CS

PBN HYSTERO-SALPINGOGRAPHY CATHETER SET

FDA registration
MedXL·1 product·🇺🇸 United States

Heightening spacers Clean

FDA registration
ETAC AB·1 product·🇸🇪 Sweden

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval
FDA Class 3 ·Senza Spinal Cord Stimulation (SCS) System and HFX iQ System