OKTAGON Dental Implant BL NC 22052

by Hager & Meisinger Gesellschaft mit beschränkter Haftung

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberEDRS220521 UDI-DI	Date2 Mar 2017Listed	StatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: OKTAGON Dental Implant BL NC
Generic Name: Screw endosteal dental implant, two-piece
Model / Ref / Catalog: 22052

Primary DI / UDI-DI: EDRS220521
510(k) Number: K162073
FDA Product Code: DZE
GMDN Term: Screw endosteal dental implant, two-piece

Device Class: Class II
Regulation Number: 872.3640
GUDID distribution status: Not in Commercial Distribution

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Class I

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Properties

Sterile
Single Use
Implantable
Prescription Use
Lot / Batch Number
Expiration Date

Other properties (8)

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