# LuxCreo, Inc.

- Location (FDA's records): Chicago, IL
- FDA decisions: 5 (2022–2026): 5 510(k) clearances
- Product codes: NXC (2), MQC (1), EBI (1), PNN (1)
- 510(k) review time since 2016: median 256 days, against 98 for FDA's reviews in the same codes and years (1 of 5 faster)
- Predicates its devices cite: 5 (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
- Ulab Systems, Inc.: 1 (https://510kreport.com/company/ulab-systems)
- Clearcorrect, LLC: 1 (https://510kreport.com/company/clearcorrect)
- Sprintray, Inc.: 1 (https://510kreport.com/company/sprintray)
- Keystone Industries: 1 (https://510kreport.com/company/keystone-industries)

## Firms that cite its devices most
- Dreve Dentamid GmbH: 1 (https://510kreport.com/company/dreve-dentamid)
- Aidite (Qinhuangdao) Technology Co., Ltd.: 1 (https://510kreport.com/company/aidite-qinhuangdao-technology)

## Its most-cited devices
- K212680: LuxCreo Clear Aligner System (2022), cited by 3

## Recent decisions
- K260421: LuxDesign (Oct 23, 2026)
- K253365: LuxCreo Flexible Partial Denture Resin (Nov 25, 2025)
- K250343: LuxCreo Clear Aligner System (Apr 8, 2025)
- K230592: LuxCreo Dental Night Guard Resin (Jan 18, 2024)
- K212680: LuxCreo Clear Aligner System (May 31, 2022)

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