OCTAGON Infinity BL NC Abutment angled 18° GH 3 mm 5022026

GUDID E0HM50220261

BL NC Abutment angled 18° GH 3 mm for OCTAGON Infinity Dental Implant BL NC

Hager & Meisinger Gesellschaft mit beschränkter Haftung

Dental implant suprastructure, permanent, preformed
Primary Device IDE0HM50220261
NIH Device Record Key60c90d85-5d58-481b-8dc9-5bb65229e6cb
Commercial Distribution StatusIn Commercial Distribution
Brand NameOCTAGON Infinity BL NC Abutment angled 18° GH 3 mm
Version Model Number5022026
Catalog Number5022026
Company DUNS318034329
Company NameHager & Meisinger Gesellschaft mit beschränkter Haftung
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 Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com
Phone+1(503)588-3100
Emailkathystrange@acesurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCE0HM50220261 [Primary]
HIBCCE0HM50220269 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


[E0HM50220261]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-08
Device Publish Date2017-01-24

Devices Manufactured by Hager & Meisinger Gesellschaft mit beschränkter Haftung

E0HM2449LKR317012101 - Bone Management2025-03-24 HARTMETALLFIN. - FG
E0HM36GF0800622801 - n/a2025-03-24 Surgical Guide Fixation Screw
E0HM39BMP0000161 - Bone Management2025-03-24 Screwdriver T6 L76.1
E0HM39BMP0000171 - Bone Management2025-03-24 Screwdriver T6 L56.1
E0HM510833L317018101 - Bone Management2025-03-24 DIAMANTINSTR. - FG
E0HM7100001204005101 - n/a2025-03-24 HARTMETALLBO. - W myone
E0HM7100001204006101 - n/a2025-03-24 HARTMETALLBO. - W myone
E0HM7100001204008101 - n/a2025-03-24 HARTMETALLBO. - W myone

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.