# Spartronics Watertown LLC (contract manufacturer, Watertown, SD): 6 new FDA device listings, incl. stimulator, spinal-cord, totally implanted for pain relief

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Spartronics Watertown LLC |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Watertown, SD, US |
| New listings | 6 |
| Devices | Stimulator, Spinal-Cord, Totally Implanted For Pain Relief; Stimulator, Spinal-Cord, Totally Implanted For Relief Of Pain Due To Diabetic Neuropathy; Stimulator, Electrical, Implanted, For Essential Tremor; Stimulator, Electrical, Implanted, For Parkinsonian Tremor; Stimulator, Electrical, Implanted, For Parkinsonian Symptoms; Needle, Hypodermic, Single Lumen |
| Product codes | LGW, QRB, PJS, MHY, NHL, FMI |
| Device classes | Class II, Class III |
| Medical specialties | General Hospital |
| Brand names | Charger Kit, Lumbar – 36000; Charger – 16000; SCS Charging System – 36700; Liberta RC Charger Kit – 66000; DBS Charging System – 66700; Arrow EZ-IO G3 Power Driver (Civilian); Arrow EZ-IO G3 Power Driver (Military) |
| First new listing | 2026-05-21 |
| Latest new listing | 2026-07-30 |
| FDA registration number | 2133772 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- 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.