DavisDuhs, LLC

FDA Device Registration & Listing · Auburn, CA, US · Registration 3038700860

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
3038700860
FEI Number
3038700860
Entity Name
DavisDuhs, LLC
City/State/Country
Auburn, CA, US
Establishment Address
1476 Grass Valley Hwy, Auburn, CA 95603, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device
Owner / Operator
DavisDuhs, LLC (Owner Number: 10093390)
Owner / Operator Contact Address
1476 Grass Valley Hwy, Auburn, CA 95603, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BUE Bottoms Up Enemas

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FCE Enema Kit Gastroenterology, Urology Class 1 876.5210 2025-05-28

Official Correspondent

Laura Davis

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DavisDuhs, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038700860. Last updated year: 2026. Please use registration number 3038700860 when referencing this establishment in official correspondence.
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