ENLITIC, INC.

FDA Device Registration & Listing · Loveland, CO, US · Registration 3014300962

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014300962
FEI Number
3014300962
Entity Name
ENLITIC, INC.
City/State/Country
Loveland, CO, US
Establishment Address
1635 Foxtrail Drive, Suite 111A, Loveland, CO 80538, US
Establishment Type(s)
Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Enlitic (Owner Number: 10062523)
Owner / Operator Contact Address
1635 Foxtrail Drive, Suite 111A, Loveland, CO 80538, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ENDEX Ensight

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LMD System, Digital Image Communications, Radiological Radiology Class 1 892.2020 2020-02-06

Official Correspondent

Treya Collins

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Enlitic
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3009227717 LAITEK INC. Loveland, CO, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014300962. Last updated year: 2026. Please use registration number 3014300962 when referencing this establishment in official correspondence.
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