HIGHER DOSE LLC

FDA Device Registration & Listing · Brentwood, CA, US · Registration 3019734322

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
3019734322
FEI Number
3019734322
Entity Name
HIGHER DOSE LLC
City/State/Country
Brentwood, CA, US
Establishment Address
3130 Balfour Rd Ste D - 516, Brentwood, CA 94513, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Higher Dose LLC (Owner Number: 10082327)
Owner / Operator Contact Address
3130 Balfour Rd, Ste D - 516, Brentwood, CA 94513, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HIGHERDOSE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IRT Pad, Heating, Powered Physical Medicine Class 2 890.5740 2023-03-03

Official Correspondent

Sumish Khadka

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Higher Dose 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
K881862 Thermo Body Wrap Systems, Inc. THERMO-BODY-WRAP SYSTEM 1988-10-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3019734322. Last updated year: 2026. Please use registration number 3019734322 when referencing this establishment in official correspondence.
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