Deebo Warehouse

FDA Device Registration & Listing · Raleigh, NC, US · Registration 3030410270

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
3030410270
FEI Number
3030410270
Entity Name
Deebo Warehouse
City/State/Country
Raleigh, NC, US
Establishment Address
3915 Beryl Road, Suite 120, Raleigh, NC 27609, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Deebo LLC (Owner Number: 10089989)
Owner / Operator Contact Address
109 Dartmouth Road, Raleigh, NC 27609, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Deebo Otoscope Kit Deebo Specula

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ERA Otoscope Ear, Nose, Throat Class 1 874.4770 2024-01-31
EPY Speculum, Ent General, Plastic Surgery Class 1 878.1800 2024-01-31

Official Correspondent

Minni Marwaha

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K932506 Rudolf Riester GmbH & Co. KG RI-SCOPE (S) 1993-10-08
K834189 Imm Enterprises , Ltd. JAKOBI SURG. INSTRUMENTS #7 44/47 1984-03-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030410270. Last updated year: 2026. Please use registration number 3030410270 when referencing this establishment in official correspondence.
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