# Sientra, Inc.

- Location (FDA's records): Santa Barbara, CA
- FDA decisions: 3 (2020–2023): 3 510(k) clearances
- Product codes: LCJ (2), MRD (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (0 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
- Mentor Corp.: 1 (https://510kreport.com/company/mentor)
- Motiva USA, LLC: 1 (https://510kreport.com/company/motiva-usa)
- Specialty Surgical Products, Inc.: 1 (https://510kreport.com/company/specialty-surgical-products)

## Recent decisions
- K214124: AlloX2 Pro Tissue Expanders (Jun 8, 2023)
- K221127: Sientra, inc. Portfinder (May 10, 2023)
- K200706: Sientra OPUS Silicone Gel Breast Implant Sizer (Nov 16, 2020)

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