PATHFINDER NXT MINIMALLY INVASIVE PEDICLE SCREW SYSTEM Bridges (implant borne)

by Institut Straumann SA 36 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number07630031704535 UDI-DI	Date24 Aug 2019Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Pathfinder Nxt Minimally Invasive Pedicle Screw System
Generic Name: Dental implant suprastructure, permanent, preformed
Model / Ref / Catalog: Bridges (implant borne), 010.7072

Primary DI / UDI-DI: 07630031704535
FDA Product Code: EHO
GMDN Term: Dental implant suprastructure, permanent, preformed

Device Class: Class I
Regulation Number: 872.3165
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Properties

Single Use
Implantable
Prescription Use
Serial 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
Lot / Batch Number: No
Expiration Date: No
Manufacturing Date: No