Verza Guidance System 642-504

by Civco Medical Instruments Co., Inc.

Listed FDA GUDID listing, no authorization on record

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	Number00841436112079 UDI-DI	Date24 Sep 2018Listed	StatusListed GUDID: 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Withdrawn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: Verza Guidance System
Generic Name: Ultrasound imaging system tracking positioner, reusable
Model / Ref / Catalog: 642-504
Description: Reusable non-sterile Verza™ bracket for use with GE Healthcare C1-6 transducers

Primary DI / UDI-DI: 00841436112079
510(k) Number: K160806
FDA Product Code: ITX
GMDN Term: Ultrasound imaging system tracking positioner, reusable

Device Class: Class II
Regulation Number: 892.1570
GUDID distribution status: In Commercial Distribution

Size: Length — 3.21 Inch
Width — 1.2 Inch

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Properties

Prescription Use
Convenience Kit
Lot / Batch Number
Manufacturing Date

Other properties (10)

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