FYDClass II

Apparatus, Exhaust, Surgical

21 CFR 878.5070 / General, Plastic Surgery

FYD is the FDA product code for Apparatus, Exhaust, Surgical, a class II device type, regulated under 21 CFR 878.5070. As of 2026-09-10, FDA records hold 75 510(k) clearances under this code, the most recent dated 2024-08-05, and 23 recalls.

Classification record

Product code: FYD
Device name: Apparatus, Exhaust, Surgical
Regulation: 21 CFR 878.5070
Device class: Class II
Review panel: General, Plastic Surgery
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 75
Ingested recalls: 23

Clearances, product code FYD

By decision year

75 clearances under product code FYD with a decision year between 1985 and 2024, 1993 the highest year at 19.

Show the numbers

510(k) clearances under FDA product code FYD by decision year
Year	Clearances
1985	1
1988	2
1989	2
1990	2
1991	7
1992	4
1993	19
1994	4
1995	3
1997	2
1998	1
1999	6
2000	2
2001	2
2002	1
2004	1
2005	1
2006	2
2009	1
2014	1
2015	1
2017	1
2018	1
2019	3
2020	1
2021	1
2022	1
2024	2

Applicants with the most clearances

Product code FYD

Applicants holding the most 510(k) clearances under product code FYD
Applicant	Clearances
Buffalo Filter Co., Inc.	21
I.C. Medical, Inc.	5
ConMed Corporation	2
Medtronic, Inc.	2
Megadyne Medical Products, Inc	2
Quinn Healthcare Products	2
Stackhouse Assoc.	2
Acuderm, Inc.	1
American Immuno Tech	1
Bei Medical Systems Co., Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 65 companies shown, in name order