# K062725: Maxiflex-Semi Flex Scope

- Pathway: 510(k) (Traditional)
- Applicant: Technology Delivery Systems, Inc.
- Decided: Sep 29, 2006 after 16 days
- Product code: FGB (Ureteroscope And Accessories, Flexible/Rigid)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K111480: Maxiflex - Semi Flex Scope, 25 to 65 CM (2012), 0 descendants of its own

## Indications for use
The MaxiFlex Semi Flex ScopesTM are intended to be used by trained medical professionals to examine the urinary tract, and using additional accessories, to perform various diagnostic and therapeutic procedures

Source page: https://510kreport.com/device/K062725
Methodology: https://510kreport.com/methodology