# K090079: Vivid, Models 40-A0001, 40-A0004, 40-A0006

- Pathway: 510(k) (Traditional)
- Applicant: Progeny, Inc.
- Decided: May 1, 2009 after 109 days
- Product code: EIA (Unit, Operative Dental)
- Device class: 1
- Regulation: 21 CFR 872.6640
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K963778 (1996). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032904: Acucam Concept IV FWT, Model 110-0185G1, Dentsply Intl. (2003) Summary page 2.
- K963778: CDR-Cam, Schick Technologies, Inc. (1996) Summary page 2.

## Indications for use
The Vivid Intraoral Video Camera is intended to provide a dentist with the ability to view the oral cavity prior to and subsequent to dental procedures.

Source page: https://510kreport.com/device/K090079
Methodology: https://510kreport.com/methodology