# Deka Research & Development Corp. (specification developer, Manchester, NH): 4 new FDA device listings, incl. controller, infusion, intravascular, electronic

**Score:** 95/100

| Field | Value |
|---|---|
| Establishment | Deka Research & Development Corp. |
| Owner / operator | DEKA Research & Development Corp. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Develop Specifications But Do Not Manufacture At This Facility |
| Location | Manchester, NH, US |
| New listings | 4 |
| Devices | Controller, Infusion, Intravascular, Electronic; Set, Administration, Intravascular; Insulin Pump Secondary Display; Alternate Controller Enabled Insulin Infusion Pump |
| Product codes | LDR, FPA, PKU, QFG |
| Device classes | Class II |
| Medical specialties | General Hospital, Clinical Chemistry |
| Brand names | twiist Automated Insulin Delivery (AID) System Powered by Tidepool; twiist AID System |
| First new listing | 2026-05-28 |
| Latest new listing | 2026-09-25 |
| FDA registration number | 1220973 |
| Registration expires | 2027-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
- Listed in the last 45 days.

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.