Katalyst Surgical, LLC
Katalyst Surgical, LLC holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2022, with 12 FDA device recalls on record.
Top product codes for Katalyst Surgical, LLC
FDA recalls by Katalyst Surgical, LLC
10 most recent of 12- Z-2070-2026 — DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog Number: DVF4005-25
- Z-2073-2026 — DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23
- Z-2071-2026 — DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DVF4014-25-S
- Z-2074-2026 — DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-25
- Z-2069-2026 — DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
- Z-2080-2026 — DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-27
- Z-2079-2026 — DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S
- Z-2078-2026 — DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25
- Z-2077-2026 — DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-S
- Z-2075-2026 — DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-25-S
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 Katalyst Surgical, LLC
- K213610 — Kogent Disposable Copper Forceps, Kogent Disposable Irrigating Copper Forceps, Kogent Disposable Illuminating Copper Forceps
- K192963 — Kogent Torus Ultrasonic Aspirator
- K163632 — Katalyst Cyclophotocoagulation Probe
- K141781 — KOGENT SPETZLER LIGHTED SUCTION TUBES
- K140362 — KATALYST REVOLVER LASER PROBES, KATALYST REVOLVER ILLUMINATED LASER PROBES, KATALYST REVOLVER ILLUMINATED PROBES
- K123172 — KOGENT BIPOLAR FORCEPS
- K121187 — KATALYST LASER PROBES, KATALYST ILLUMINATED LASER PROBES
Data sourced from openFDA. This site is unofficial and independent of the FDA.