Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017059592

FEI Number

3017059592

Entity Name

DITEK CONSULTING LLC

City/State/Country

Glastonbury, CT, US

Establishment Address

99 Commerce St, Glastonbury, CT 06033, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Ditek Consulting LLC (Owner Number: 10075817)

Owner / Operator Contact Address

160 OAK ST STE 210, Glastonbury, CT 06033, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Ditek Collection Kit Colofit Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OIB	Blood And Urine Collection Kit (Excludes Hiv Testing)	Pathology	Class 1	864.3250	2022-11-30
NNK	Container, Specimen Mailer And Storage, Non-Sterile	Pathology	Class 1	864.3250	2024-07-03

Official Correspondent

Daniel DelMastro

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ditek Consulting LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017059592. Last updated year: 2026. Please use registration number 3017059592 when referencing this establishment in official correspondence.