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

Deka Research & Development Corp. (Manchester, New Hampshire): 4 new FDA device listings, incl. controller, infusion, intravascular, electronic. Its amount of 4 is above the median of 1 (83rd percentile). Dated 41 days ago, it serves as a historical benchmark. Score 95/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)

amount: 4 · 83th percentile of 2,570 DeviceEstablishmentPulse records · 4.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 11 related NH DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentDeka Research & Development Corp.
Owner / operatorDEKA Research & Development Corp.
RoleSpecification developer (outsources manufacturing)
Establishment typesDevelop Specifications But Do Not Manufacture At This Facility
LocationManchester, NH, US
New listings4
DevicesController, Infusion, Intravascular, Electronic; Set, Administration, Intravascular; Insulin Pump Secondary Display; Alternate Controller Enabled Insulin Infusion Pump
Product codesLDR, FPA, PKU, QFG
Device classesClass II
Medical specialtiesGeneral Hospital, Clinical Chemistry
Brand namestwiist Automated Insulin Delivery (AID) System Powered by Tidepool; twiist AID System
First new listing2026-05-28
Latest new listing2026-09-25
FDA registration number1220973
Registration expires2027-12-31
amount percentile83th of 2,570 (median 1, 4.0x median)
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL

  • Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
  • Record date: 2026-09-25
  • Data refreshed: 2026-10-28
  • Refunds on request within 14 days

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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT

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Peer benchmark and outreach value: Deka Research & Development Corp. and 12 New Hampshire peers

  • New Hampshire DeviceEstablishmentPulse records like this one: 12
  • Deka Research & Development Corp.'s amount: 83rd percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every New Hampshire peer: $2,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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95 / 100 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.

What is the DeviceEstablishmentPulse record for Deka Research & Development Corp. in Manchester, New Hampshire?

Deka Research & Development Corp. (Manchester, NH), a specification developer (outsources manufacturing), added 4 FDA device listings between 2026-05-28 and 2026-09-25.

How does Deka Research & Development Corp. compare to other New Hampshire DeviceEstablishmentPulse records?

Its amount of 4 sits in the upper half (83th percentile) of 2,570 records; the median is 1. It is 41 days old, still within a typical 45-day follow-up window. Its Score of 95/100 puts it among the stronger signals in this feed.

Deka Research & Development Corp. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Deka Research & Development Corp.Manchester, NH483rd2026-09-25
Alc Enterprises IncBrooklyn, NY483rd2026-10-18
Davol Inc., Sub. C.R. Bard, Inc.Warwick, RI377th2026-10-14
Ge Medical Systems, LLCWaukesha, WI377th2026-10-06

Related records

DeviceEstablishmentPulse: Specification developer (outsources manufacturing) DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in New Hampshire

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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.

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