Contract manufacturerKATALYST SURGICAL, LLC (Chesterfield, MO)MissouriGeneral and plastic surgeryOphthalmicClass IClass II
KATALYST SURGICAL, LLC
Contract manufacturer ยท Chesterfield, MO
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3007589150 (openFDA record; or search FDA's registration database)
- FEI number
- 3007589150
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Specification developer; Manufacturer; Contract manufacturer; Remanufacturer; Repackager or relabeler
- Owner or operator
- Katalyst Surgical, LLC (FDA owner/operator no. 10029103)
- Registered address
- 722 Goddard Ave, Chesterfield, MO 63005
- Contract listings
- 8 device listings, 8 product codes, first listed Dec 8, 2010
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| FSM | Tray, Surgical, Instrument | Class I | General and plastic surgery | Contract manufacturing | May 9, 2012 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | Class II | General and plastic surgery | Contract manufacturing | May 17, 2013 |
| HMX | Cannula, Ophthalmic | Class I | Ophthalmic | Contract manufacturing | Dec 8, 2010 |
| HNF | Scissors, Ophthalmic | Class I | Ophthalmic | Contract manufacturing | Dec 8, 2010 |
| HNN | Knife, Ophthalmic | Class I | Ophthalmic | Contract manufacturing | Dec 8, 2010 |
| HNR | Forceps, Ophthalmic | Class I | Ophthalmic | Contract manufacturing | Dec 8, 2010 |
| HTD | Forceps | Class I | General and plastic surgery | Contract manufacturing | May 15, 2012 |
| MXY | Cannula, Ophthalmic, Posterior Capsular Polishing, Polyvinyl Acetal | Class I | Ophthalmic | Contract manufacturing | May 9, 2012 |