ORTHOMED, LLC

FDA Device Registration & Listing · Whittier, CA, US · Registration 3009142693

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
3009142693
FEI Number
3009142693
Entity Name
ORTHOMED, LLC
City/State/Country
Whittier, CA, US
Establishment Address
9925 Painter Ave, Suite D, Whittier, CA 90605, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Orthomed, LLC (Owner Number: 10036783)
Owner / Operator Contact Address
9925 Painter Ave Ste D, Whittier, CA 90605, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K993420
PMA Number
N/A

All Registered Proprietary Names

myHome Rehab Exercise Kit myHome Rehab Exercise Kit Tri-Wave

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILO Pack, Hot Or Cold, Water Circulating Physical Medicine Class 2 890.5720 2011-05-25
IOD Components, Exercise Physical Medicine Class 1 890.5350 2011-05-25
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2025-02-05

Official Correspondent

Renee Smedley-Gonzalez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Orthomed, 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
K030403 Cefar Medical AB CEFAR REHAB 2 AND REHAB 2 PRO 2003-07-17
K231440 Shenzhen Roundwhale Technology Co. , Ltd. Combo Electrotherapy Device 2023-11-03
K820884 Nitron Electronics ELECTRICAL MUSCLE STIMULATOR 1982-04-29
K201958 Therasigma, LLC ETD Family of Electrotherapy Devices 2020-08-04
K964028 Mettler Electronics Corp. SYS STIM 226 1997-02-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009142693. Last updated year: 2026. Please use registration number 3009142693 when referencing this establishment in official correspondence.
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