# Lenstec, Inc.

- Location (FDA's records): St. Petersburg, FL
- FDA decisions: 8 (2005–2022): 6 510(k) clearances and 2 original PMA approvals
- Product codes: MSS (5), MFK (1), HQC (1), HQL (1)
- Predicates its devices cite: 10 (5 its own); citations of its devices by later devices: 6 (5 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
- Medicel AG: 2 (https://510kreport.com/company/medicel)
- Staar Surgical Co.: 2 (https://510kreport.com/company/staar-surgical)
- Milvella Pty., Ltd.: 1 (https://510kreport.com/company/milvella)

## Firms that cite its devices most
- Asico, LLC: 1 (https://510kreport.com/company/asico)

## Its most-cited devices
- K063802: Lenstec LC Injection System (2007), cited by 2
- K050638: Lenstec Intraocular Lens (Iol) Injection System for Tetraflex Intraocular Lenses (2005), cited by 2
- K060533: Lenstec Intraocular Lens (Iol) Injection System (2006), cited by 1
- K122848: Lenstec LC Injection System (2013), cited by 1

## Recent decisions
- P200020: SBL-3 Multifocal Intraocular Lens (Jul 22, 2022)
- K161776: Lenstec LC Injection system (Nov 29, 2016)
- K122848: Lenstec LC Injection System (Oct 18, 2013)
- P090022: Lenstec Softec HD Posterior Chamber Intraocular Lens (Apr 12, 2010)
- K091915: Fluid Isolation Device (Oct 27, 2009)
- K063802: Lenstec LC Injection System (May 7, 2007)
- K060533: Lenstec Intraocular Lens (Iol) Injection System (Apr 14, 2006)
- K050638: Lenstec Intraocular Lens (Iol) Injection System for Tetraflex Intraocular Lenses (May 31, 2005)

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