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Visix Imaging

by Televere Systems

510(k) K082623

Visix Imaging is a Class II device made by Televere Systems, cleared under FDA 510(k) K082623 on 25 Feb 2009, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK082623 Date25 Feb 2009ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
LLZ
Device class
Class II
Regulation
21 CFR Part 892.2050
Advisory committee
Radiology
FDA decision
SESE Substantially Equivalent

Devices cleared under K082623

4 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K082623
UDI-DISize and differences
Visix 2.3.9
Televere Systems
Visix 2.3.9 / 2.3.900851800007030 —On the market
Visix 7.7.15
Televere Systems
Visix Pro 7.7.15 / 7.7.1500851800007047 —On the market
Visix 8.1 Build 81
Televere Systems
Visix 8.1 Build 81 / 8.1 Build 8100851800007054 —On the market
Visix for Intraoral Camera 2.3.10
Televere Systems
Visix for Intraoral Camera 2.3.10 / for Intraoral Camera 2.3.1000851800007092 —On the market

Similar devices

Other devices filed under FDA product code LLZ (System, Image Processing, Radiological).

Other devices from Televere Systems

  • TigerView 8.6

    Class II
  • TigerView 8.1 Build 81

    Class II
  • Visix 2.3.9

    Class II
  • Visix 7.7.15

    Class II

See all devices from Televere Systems →