FZSClass I

Curette, Surgical, General Use

21 CFR 878.4800 / General, Plastic Surgery

FZS is the FDA product code for Curette, Surgical, General Use, a class I device type, regulated under 21 CFR 878.4800. As of 2026-09-10, FDA records hold 14 510(k) clearances under this code, the most recent dated 1994-01-07, and 3 recalls.

Classification record

Product code: FZS
Device name: Curette, Surgical, General Use
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: 14
Ingested recalls: 3

Clearances, product code FZS

By decision year

14 clearances under product code FZS with a decision year between 1981 and 1994, 1989 the highest year at 4.

Show the numbers

510(k) clearances under FDA product code FZS by decision year
Year	Clearances
1981	1
1983	2
1984	1
1985	2
1987	1
1988	1
1989	4
1990	1
1994	1

Applicants with the most clearances

Product code FZS

Applicants holding the most 510(k) clearances under product code FZS
Applicant	Clearances
Euro-Med Intl.	2
3M Company	1
Acuderm, Inc.	1
Arthropedics, Inc.	1
Cymed, Inc.	1
Downs Surgical, Ltd.	1
Kevtek Medical Products, Inc.	1
Kinetic Medical Products	1
Pmt, Inc.	1
T. Korossurgical Instruments Corp.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 211 companies shown, in name order