# Katalyst Surgical, LLC

- Location (FDA's records): Chesterfield, MO
- FDA decisions: 7 (2012–2022): 7 510(k) clearances
- Product codes: HQF (2), GEI (2), HBI (1), LQJ (1), LFL (1)
- Predicates its devices cite: 12 (2 its own); citations of its devices by later devices: 4 (2 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
- Synergetics, Inc.: 4 (https://510kreport.com/company/synergetics)
- Ophthalmed, LLC: 2 (https://510kreport.com/company/ophthalmed)
- Invuity, Inc.: 1 (https://510kreport.com/company/invuity)
- Iridex Corp: 1 (https://510kreport.com/company/iridex)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Mutoh America Co., Ltd.: 1 (https://510kreport.com/company/mutoh-america)

## Firms that cite its devices most
- VitreQ BV: 1 (https://510kreport.com/company/vitreq)
- Ophthalmed, LLC: 1 (https://510kreport.com/company/ophthalmed)

## Its most-cited devices
- K121187: Katalyst Laser Probes, Katalyst Illuminated Laser Probes (2012), cited by 3
- K123172: Kogent Bipolar Forceps (2012), cited by 1

## Recent decisions
- K213610: Kogent Disposable Copper Forceps, Kogent Disposable Irrigating Copper Forceps, Kogent Disposable Illuminating Copper Forceps (Oct 7, 2022)
- K192963: Kogent Torus Ultrasonic Aspirator (Jun 19, 2020)
- K163632: Katalyst Cyclophotocoagulation Probe (Jun 15, 2017)
- K141781: Kogent Spetzler Lighted Suction Tubes (Apr 9, 2015)
- K140362: Katalyst Revolver Laser Probes, Katalyst Revolver Illuminated Laser Probes, Katalyst Revolver Illuminated Probes (Sep 15, 2014)
- K123172: Kogent Bipolar Forceps (Dec 21, 2012)
- K121187: Katalyst Laser Probes, Katalyst Illuminated Laser Probes (Sep 17, 2012)

Source page: https://510kreport.com/company/katalyst-surgical