Establishment registration
KATALYST SURGICAL, LLC
FDA establishment registration 3007589150 · Chesterfield, US
Key facts
| Registration number | 3007589150 |
|---|---|
| Establishment name | KATALYST SURGICAL, LLC |
| Owner/operator | Katalyst Surgical, LLC |
| Owner/operator number | 10029103 |
| FEI number | 3007589150 |
| Address | 722 Goddard Ave |
| City | Chesterfield |
| State | MO |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | EMF, FFS, FSM, FST, FZS, GAD, GDF, GDG, GEI, HAO, HBI, HCF, HMR, HMX, HMZ, HNC, HND, HNF, HNH, HNI, HNJ, HNN, HNQ, HNR, HNW, HNX, HOE, HQB, HQF, HTD and 6 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- 1–9 FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database