X-Guide P010727

by X-Nav Technologies, LLC

X-Guide P010727 is a Class II device made by X-Nav Technologies, LLC, listed in FDA GUDID since 3 Feb 2021 (UDI-DI 00817421021503), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00817421021503 UDI-DI	Date3 Feb 2021Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00817421021503

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: X-Guide
Generic name: Surgical planning/navigation-enhancement system
Model / reference: P010727

Primary DI / UDI-DI: 00817421021503
FDA product code: PLV
GMDN term: Surgical planning/navigation-enhancement system

Device class: Class II
Regulation number: 872.4120
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Lot / batch number

Other properties (12, all answered No)