Alcon Research, Ltd.
Alcon Research, Ltd. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2017, with 39 FDA device recalls on record.
Top product codes for Alcon Research, Ltd.
FDA recalls by Alcon Research, Ltd.
10 most recent of 39- Z-2409-2023 — Legion FMS Pak
- Z-2407-2023 — Centurion FMS Pak
- Z-2411-2023 — Alcon Custom Pak
- Z-2410-2023 — Phaco Standalone Tips
- Z-2406-2023 — Constellation Procedure Pak
- Z-2408-2023 — Infinity FMS Pak
- Z-0187-2019 — CyPass ULTRA SYSTEM, CYPASS MICRO-STENT, CYPASS APPLIER, REF CATALOG #: 8065754007. For ophthalmic use.
- Z-0188-2019 — CyPass System 241, Intraocular Pressure Lowering Implant, CYPASS MICRO-STENT, CYPASS APPLIER, REF: 8065754010. For ophthalmic use.
- Z-0186-2019 — CyPass System 241, Intraocular Pressure Lowering Implant, CYPASS MICRO-STENT, CYPASS APPLIER, REF: 8065754001. For ophthalmic use.
- Z-0185-2019 — CyPass System 241-S, CYPASS MICRO-STENT, CYPASS LOADED, CYPASS APPLIER, REF CATALOG #: 8065754003 For ophthalmic use.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Alcon Research, Ltd.
- K161794 — CENTURION Vision System (Active SentryTM)
- K170520 — HyperVit Vitrectomy Probe, 23 GA, HyperVit Vitrectomy Probe, 25+, HyperVit Vitrectomy Probe, 27+
- K141065 — CONSTELLATION VISION SYSTEM
- K121031 — WAVELIGHT FS200 PATIENT INTERFACE 1505
- K112977 — MONARCH III IOL DELIVERY SYSTEM, MONARCH III C CARTRIDGE, MONARCH III HANDPIECE (H4)
- K110951 — 27+ ULTRAVIT PROBE, 27+ FLEX-TIP LASER PROBE, 27+ ENDOILLUMINATOR PROBE, 27+ VALVED ENTRY SYSTEM, 27+ INFUSION CANNULA
- K110166 — CLEARCUT S SAFETY KNIFE
- K102860 — ALCON MULTI-PIRPOSE DISINFECTING SOLUTION
- K101006 — WAVELIGHT FS200 LASER SYSTEM MODEL: FS200
- K093305 — ENHANCED ULTRA VIT PROBE
- K091777 — ALCON ULTRACHOPPER
- K082845 — INFINITI VISION SYSTEM WITH OZIL IP
- K062930 — LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM
- K050729 — ALCON MULTI-PURPOSE DISINFECTING SOLUTION
- K003768 — MONARCH II IOL DELIVERY SYSTEM
- K001157 — MONARCH II IOL DELIVERY SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.