HOME AIDE DIAGNOSTICS, INC.

FDA Device Registration & Listing · Deerfield Bch, FL, US · Registration 3005750815

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
3005750815
FEI Number
3008474962
Entity Name
HOME AIDE DIAGNOSTICS, INC.
City/State/Country
Deerfield Bch, FL, US
Establishment Address
1072 S Powerline Rd, Deerfield Bch, FL 33442, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
HOME AIDE DIAGNOSTICS, INC. (Owner Number: 9087599)
Owner / Operator Contact Address
1072 S. Powerline Rd., --, Deerfield Bch, FL 33442, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pro Comfort Alcohol prep pads True Comfort Alcohol Prep Pads True Comfort Pro Alcohol Prep Pads

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LKB Pad, Alcohol, Device Disinfectant Unknown Class U N/A 2015-01-26

Official Correspondent

AMGAD GIRGIS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HOME AIDE DIAGNOSTICS, 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
3006899020 HUAIAN HENING MEDICAL INSTRUMENTS CO ., LTD and its Subsidiary HUAIAN JUNRAN IMP.&EXP. TRADING CO.,LTD Huaian Jiangsu, CN

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005750815. Last updated year: 2026. Please use registration number 3005750815 when referencing this establishment in official correspondence.
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