LAITEK INC.

FDA Device Registration & Listing · Loveland, CO, US · Registration 3009227717

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
3009227717
FEI Number
3009227717
Entity Name
LAITEK INC.
City/State/Country
Loveland, CO, US
Establishment Address
1635 Foxtrail Drive, Suite 111B, Loveland, CO 80538, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
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

Semperdata® ATRIUM® ATRIUM® Route ATRIUM® Import ATRIUM® Keep MIGRATEK®

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OUG Medical Device Data System General Hospital Class 1 880.6310 2024-11-15

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
3014300962 ENLITIC, 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 3009227717. Last updated year: 2026. Please use registration number 3009227717 when referencing this establishment in official correspondence.
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