# K080735: Cryomini

- Pathway: 510(k) (Special)
- Applicant: Zimmer Elektromedizin GmbH
- Decided: Apr 4, 2008 after 18 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K963094 (1996). 37 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 39 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060395: Cryo, Model V6.0, Zimmer Elektromedizin GmbH (2006) Summary page 1.

## Most influential descendants
- K090618: Cynosure Smartcool Family Cold Air Device: Smartcool, Smartcool 6 and Cryo C (2009), 0 descendants of its own

## Indications for use
The CryoMini Cold Air Device is intended to minimize pain and thermal injury during laser and dermatological treatments and for temporary topical anesthetic relief for injections.

Source page: https://510kreport.com/device/K080735
Methodology: https://510kreport.com/methodology