DIAMOND ORTHOTIC LABORATORY, LLC

FDA Device Registration & Listing · La Mesa, CA, US · Registration 3012728846

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
3012728846
FEI Number
3012728846
Entity Name
DIAMOND ORTHOTIC LABORATORY, LLC
City/State/Country
La Mesa, CA, US
Establishment Address
7859 El Cajon Blvd., La Mesa, CA 91942, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Diamond Orthotic Laboratory, LLC (Owner Number: 10059263)
Owner / Operator Contact Address
7859 El Cajon Blvd., La Mesa, CA 91942, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DDSO (Diamond Digital Sleep Orthotic) SnoreHook

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRK Device, Anti-Snoring Dental Class 2 872.5570 2020-09-09
LRK Device, Anti-Snoring Dental Class 2 872.5570 2018-12-16

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Diamond Orthotic Laboratory, 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
K122391 Medtronic Xomed, Inc. MEDTRONIC XOMED, INC. 2013-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012728846. Last updated year: 2026. Please use registration number 3012728846 when referencing this establishment in official correspondence.
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