Bausch & Lomb
Bausch & Lomb holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2017.
Name variants for Bausch & Lomb
as filed with FDA- Bausch & Lomb
- Bausch+Lomb
Top product codes for Bausch & Lomb
Recent clearances by Bausch & Lomb
- K170052 — Stellaris Elite vision enhancement system
- K162342 — Stellaris Elite Vision Enhancement System
- K133486 — STELLARIS PC VISION ENHANCEMENT SYSTEM
- K133242 — STELLARIS VISION ENHANCEMENT SYSTEM
- K131958 — BAUSCH & LOMB INJECTOR SYSTEM
- K133146 — BAUSCH + LUMB, VIS100 INJECTOR SYSTEM
- K132481 — EASY-LOAD LENS DELIVERY SYSTEM
- K132593 — CRYSTALSERT DELIVERY SYSTEM
- K123736 — CRYSTALSERT DELIVERY SYSTEM
- K061157 — SOFLENS ONE DAY PLUS DISPOSABLE (HILAFILCON B) VISIBILITY TINTED CONTACT LENS
- K040913 — NGDI (NEXT GENERATION DIAGNOSTIC INSTRUMENT)
- K020927 — BAUSCH & LOMB SOFLENS MULTIFOCAL (POLYMACON) VISIBILITY TINTED CONTACT LENS
Data sourced from openFDA. This site is unofficial and independent of the FDA.