KOHNO STRAIGHT IMPLANT ZT K-ZT-380-150

GUDID D7701125433

KOHNO STRAIGHT IMPLANT ZT D.3.80 H.15 MM

SWEDEN & MARTINA SPA

Screw endosteal dental implant, two-piece
Primary Device IDD7701125433
NIH Device Record Key60da932d-6a6d-4d2e-9ac2-88decf2dcc8b
Commercial Distribution StatusIn Commercial Distribution
Brand NameKOHNO STRAIGHT IMPLANT ZT
Version Model NumberK-ZT-380-150
Catalog NumberK-ZT-380-150
Company DUNS433815198
Company NameSWEDEN & MARTINA SPA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD7701125433 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DZEImplant, Endosseous, Root-Form

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-07-07
Device Publish Date2022-06-29

On-Brand Devices [KOHNO STRAIGHT IMPLANT ZT]

D7701125443KOHNO STRAIGHT IMPLANT ZT D.3.80 H.18 MM
D7701125433KOHNO STRAIGHT IMPLANT ZT D.3.80 H.15 MM
D7701125423KOHNO STRAIGHT IMPLANT ZT D.3.80 H.13 MM
D7701125413KOHNO STRAIGHT IMPLANT ZT D.3.80 H.11.5 MM
D7701125403KOHNO STRAIGHT IMPLANT ZT D.3.80 H.10 MM

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.