Visura TEECAD Carrier Control Unit VS-V2

by Visura Technologies, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 22 Oct 2026

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	Number00860226002536 UDI-DI	Date26 Jul 2022Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Visura TEECAD Carrier Control Unit
Generic Name: Ultrasound imaging transducer positioning unit
Model / Ref / Catalog: VS-V2, VIS0101

Primary DI / UDI-DI: 00860226002536
510(k) Number: K180911
FDA Product Code: ITX, FDS
GMDN Term: Ultrasound imaging transducer positioning unit

Device Class: Class II
Regulation Number: 892.1570, 876.1500
GUDID distribution status: In Commercial Distribution

MRI Safety: MR Unsafe

Other devices from Visura Technologies, LLC

Visura TEECAD Carrier CR-P2

Class II
Visura Technologies TEECAD System

Class II

Properties

Prescription Use
Serial Number
Manufacturing Date

Other properties (11)

Sterile: No
Single Use: No
Implantable: 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