OKTAGON TL RP Abutment angled 15° A H= 6.7 mm cementable 38118

by Hager & Meisinger Gesellschaft mit beschränkter Haftung 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberE0HM381181 UDI-DI	Date28 Jun 2021Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: OKTAGON TL RP Abutment angled 15° A H= 6.7 mm cementable
Generic Name: Dental implant suprastructure, permanent, preformed
Model / Ref / Catalog: 38118

Primary DI / UDI-DI: E0HM381181
FDA Product Code: NHA
GMDN Term: Dental implant suprastructure, permanent, preformed

Device Class: Class II
Regulation Number: 872.3630
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Properties

Single Use
Implantable
Prescription Use
Lot / Batch Number

Other properties (10)

Sterile: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No