LYHClass I

Arthrometer

21 CFR 890.1615 / Physical Medicine

LYH is the FDA product code for Arthrometer, a class I device type, regulated under 21 CFR 890.1615. As of 2026-09-10, FDA records hold 5 510(k) clearances under this code, the most recent dated 1995-03-02, and no recalls.

Classification record

Product code: LYH
Device name: Arthrometer
Regulation: 21 CFR 890.1615
Device class: Class I
Review panel: Physical Medicine
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 5
Ingested recalls: 0

Clearances, product code LYH

By decision year

5 clearances under product code LYH with a decision year between 1981 and 1995, 1981 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code LYH by decision year
Year	Clearances
1981	1
1984	1
1988	1
1994	1
1995	1

Applicants with the most clearances

Product code LYH

Applicants holding the most 510(k) clearances under product code LYH
Applicant	Clearances
Medmetric Corp.	3
Dyonics, Inc.	1
Far Orthopedics, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code LYH.

Recent clearances

Product code LYH

Recent recalls

Product code LYH

FDA records show no recalls under product code LYH.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)