# K980474: Telicam

- Pathway: 510(k) (Traditional)
- Applicant: Dental/Medical Diagnostic Systems, Inc.
- Decided: Apr 13, 1998 after 66 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K991011: Orascope (1999), 1 descendant of its own
- K093785: Modular Endoscope (2010), 0 descendants of its own

## Indications for use
Non diagnostic intraoral camera used by dentists to illuminate and magnify dental surfaces.

Source page: https://510kreport.com/device/K980474
Methodology: https://510kreport.com/methodology