# Linemaster Switch Corp. (contract manufacturer, Woodstock, CT): 7 new FDA device listings, incl. system, surgical, computer controlled instrument

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Linemaster Switch Corp. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Woodstock, CT, US |
| New listings | 7 |
| Devices | System, Surgical, Computer Controlled Instrument; Electrosurgical, Cutting & Coagulation & Accessories; Endoscope, Neurological; Nasopharyngoscope (Flexible Or Rigid); Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece |
| Product codes | NAY, GEI, GWG, EOB, ERL |
| Device classes | Class II |
| Medical specialties | Gastroenterology, Urology, General, Plastic Surgery, Neurology, Ear, Nose, Throat |
| Brand names | 323863 (single-pedal auxiliary footswitch) and 323864 (dual-pedal auxiliary footswitch); Hydro Foot Switch; RFP-Footswitch |
| First new listing | 2026-06-01 |
| Latest new listing | 2026-06-25 |
| FDA registration number | 3001592626 |
| 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.