510(k) Report

FDA applicant

Diamond Orthotic Laboratory

La Mesa, CA1 decision2020–20200 recalls

FDA records 1 decision for Diamond Orthotic Laboratory (La Mesa, CA) in 2020: 1 510(k) clearance. All are in product code LRK (Device, Anti-Snoring). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Diamond Orthotic Laboratory’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2020: 1
2020high 1 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Diamond Orthotic Laboratory by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LRKDevice, Anti-Snoring1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K202499Diamond Digital Sleep Orthotic (DDSO)Diamond Orthotic Laboratory · 2020

The one decision as Diamond Orthotic Laboratory →

Other applicant names beginning “Diamond”

FDA records each applicant name separately; these may or may not be the same firm.

Diamond Diagnostics, Inc. 26Diamond Medical, Inc. 6Diamond Sensor Systems 3Diamond Medical Equipment, Inc. 3Diamond Shamrock Corp. 2Diamond Electro-Tech, Inc. 1Diamond Orthopedic, LLC 1Diamond Rotary and Carbide Intl. 1Diamond Systems USA, Inc. 1Diamond Age Systems, Inc. 1Diamond General Development Corp. 1Diamond Mark International Co., Ltd. 1