ZZ BASE NE-PA-ICSC 3.5 - 4.0 - 4.5 - 5.0 - 5.5 Tapered (Impression cop BSFE3902

by Zirkonzahn GmbH

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	NumberD800BSFE3902 UDI-DI	Date27 Sep 2021Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: ZZ BASE NE-PA-ICSC 3.5 - 4.0 - 4.5 - 5.0 - 5.5 Tapered (Impression cop
Generic Name: Dental implant suprastructure, temporary, preformed, reusable
Model / Reference: BSFE3902
Description: Compatible with Neoss ProActive implants Consisting of: 1x Screw for impression copings

Primary DI / UDI-DI: D800BSFE3902
FDA Product Code: NDP
GMDN Term: Dental implant suprastructure, temporary, preformed, reusable

Device Class: Class I
Regulation Number: 872.3980
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

Other devices from Zirkonzahn GmbH

Colour Liquid A1 (20 ml) FMAA0103

Class II
Colour Liquid A3, 5 (20 ml) FMAA0403

Class II
Colour Liquid B1 (20 ml) FMAA0603

Class II
Colour Liquid A4 (20 ml) FMAA0503

Class II
Colour Liquid B2 (20 ml) FMAA0703

Class II
Colour Liquid B3 (20 ml) FMAA0803

Class II

See all devices from Zirkonzahn GmbH →

Properties

Implantable
Prescription Use
Premarket Exempt
Lot / Batch Number
Manufacturing Date

Other properties (9)

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