LRYClass I

Punch, Surgical

21 CFR 878.4800 / General, Plastic Surgery

LRY is the FDA product code for Punch, Surgical, a class I device type, regulated under 21 CFR 878.4800. As of 2026-09-10, FDA records hold 7 510(k) clearances under this code, the most recent dated 1994-03-24, and 6 recalls.

Classification record

Product code: LRY
Device name: Punch, Surgical
Regulation: 21 CFR 878.4800
Device class: Class I
Review panel: General, Plastic Surgery
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 7
Ingested recalls: 6

Clearances, product code LRY

By decision year

7 clearances under product code LRY with a decision year between 1987 and 1994, 1987 the highest year at 3.

Show the numbers

510(k) clearances under FDA product code LRY by decision year
Year	Clearances
1987	3
1990	2
1991	1
1994	1

Applicants with the most clearances

Product code LRY

Applicants holding the most 510(k) clearances under product code LRY
Applicant	Clearances
Med-Tool, Inc.	3
Acuderm, Inc.	1
Kramer Const	1
Lipogen, Inc.	1
Premier Medical	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 235 companies shown, in name order