# Katecho LLC (contract manufacturer, Des Moines, IA): 2 new FDA device listings, incl. temporarily implanted peripheral nerve stimulation system for sustaine

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Katecho LLC |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Des Moines, IA, US |
| New listings | 2 |
| Devices | Temporarily Implanted Peripheral Nerve Stimulation System For Sustained Pain Relief; Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief |
| Product codes | SCN, NHI |
| Device classes | Class II |
| Medical specialties | Neurology |
| First new listing | 2026-05-08 |
| Latest new listing | 2026-07-17 |
| FDA registration number | 1930027 |
| Registration expires | 2027-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.