Lumea, Cedar City

FDA Device Registration & Listing · Cedar City, UT, US · Registration 3016008117

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
3016008117
FEI Number
3016008117
Entity Name
Lumea, Cedar City
City/State/Country
Cedar City, UT, US
Establishment Address
309 N 200 W, Cedar City, UT 84721, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Leavitt Medical, Inc. (Owner Number: 10045889)
Owner / Operator Contact Address
2889 W Ashton Blvd Ste 300, Lehi, UT 84048, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tissue holder, transport, fixation/preservation device - BxBoard Tissue holder, transport, fixation/preservation device - BxCollect

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NNI Container, Specimen, Non-Sterile Pathology Class 1 864.3250 2016-05-02

Official Correspondent

Kyron Nielsen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3012104009 Leavitt Medical, Inc. Lehi, UT, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016008117. Last updated year: 2026. Please use registration number 3016008117 when referencing this establishment in official correspondence.
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