# Ziip,Llc

- Location (FDA's records): Piedmont, CA
- FDA decisions: 2 (2017–2021): 2 510(k) clearances
- Names in FDA's records: Ziip,Llc (1); Ziip, Inc. (1)
- Product codes: NFO (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Carol Cole Company: 1 (https://510kreport.com/company/carol-cole)
- Carol Cole Company Dba Nuface: 1 (https://510kreport.com/company/carol-cole-company-dba-nuface)

## Firms that cite its devices most
- Shenzhen Kaiyan Medical Equipment Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-kaiyan-medical-equipment)
- Johari Digital Healthcare, Ltd.: 1 (https://510kreport.com/company/johari-digital-healthcare)

## Its most-cited devices
- K212342: ZIIP+ Device (2021), cited by 2
- K161484: ZIIP Device (2017), cited by 1

## Recent decisions
- K212342: ZIIP+ Device (Sep 23, 2021)
- K161484: ZIIP Device (Feb 24, 2017)

Source page: https://510kreport.com/company/ziip