Spirulina Production Facility

FDA Device Registration & Listing · Franklin, TN, US · Registration 3011592854

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
3011592854
FEI Number
3010484784
Entity Name
Spirulina Production Facility
City/State/Country
Franklin, TN, US
Establishment Address
318 Seaboard Lane, Suite 313, Franklin, TN 37067, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Advanced Breath Diagnostics, LLC (Owner Number: 10049228)
Owner / Operator Contact Address
105 Westpark Drive, Suite 150, Brentwood, TN 37027, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P110015

All Registered Proprietary Names

13C-Spirulina GEBT 13C-Spirulina Gastric Emptying Breath Test (GEBT) 13C-Spirulina Gastric Emptying Breath Test (GEBT)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PGE Gastric Emptying Breath Test Unknown Class 3 N/A 2015-04-30

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Advanced Breath Diagnostics, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3010031043 CAIRN DIAGNOSTICS Brentwood, TN, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011592854. Last updated year: 2026. Please use registration number 3011592854 when referencing this establishment in official correspondence.
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