Visix Imaging
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
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK082623 | Date25 Feb 2009 | StatusActive |
Official records
- FDA 510(k) database K082623
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 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
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.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| Visix 2.3.9 | Visix 2.3.9 / 2.3.9 | 00851800007030 | — | On the market |
| Visix 7.7.15 | Visix Pro 7.7.15 / 7.7.15 | 00851800007047 | — | On the market |
| Visix 8.1 Build 81 | Visix 8.1 Build 81 / 8.1 Build 81 | 00851800007054 | — | On the market |
| Visix for Intraoral Camera 2.3.10 | Visix for Intraoral Camera 2.3.10 / for Intraoral Camera 2.3.10 | 00851800007092 | — | On the market |
Similar devices
Other devices filed under FDA product code LLZ (System, Image Processing, Radiological).
- LungPoint Virtual Bronchoscopic Navigation (VBN) Software by BRONCUS MEDICAL INC.
- ESIE APPS SUITE by SIEMENS MEDICAL SOLUTIONS USA, INC.
- FEEL-DRCS by Imfou Co., Ltd.
- 4D SONO-SCAN 1.0 by Tomtec Imaging Systems GmbH
- VISTADENT AT COMPLETE, MODEL 3.1 by Dentsply Intl.
- CORONIS 5MP by Barco N.V.
- SURGERY REHEARSAL PLATFORM by SURGICAL THEATER LLC
- AIDA HD CONNECT WITH SMARTSCREEN / BLU-RAY DRIVE / SMARTSCREEN WITH BLU-RAY DRIVE by Karl Storz Endoscopy-America, Inc.
- Minimally Invasive Prostate Surgery Navigation System by Augment Intelligent Medical System (China) Co., Ltd.
- RESOLUTIONMD CARDIAC PRODUCT FAMILY, MODEL: RELEASE 1.0 by Calgary Scientific, Inc.