EGSClass I

Handpiece, Contra- And Right-Angle Attachment, Dental

21 CFR 872.4200 / Dental

EGS is the FDA product code for Handpiece, Contra- And Right-Angle Attachment, Dental, a class I device type, regulated under 21 CFR 872.4200. As of 2026-09-10, FDA records hold 73 510(k) clearances under this code, the most recent dated 2025-09-15, and 2 recalls.

Classification record

Product code: EGS
Device name: Handpiece, Contra- And Right-Angle Attachment, Dental
Regulation: 21 CFR 872.4200
Device class: Class I
Review panel: Dental
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 73
Ingested recalls: 2

Clearances, product code EGS

By decision year

73 clearances under product code EGS with a decision year between 1978 and 2025, 1995 the highest year at 6.

Show the numbers

510(k) clearances under FDA product code EGS by decision year
Year	Clearances
1978	3
1979	2
1980	2
1982	1
1985	3
1993	1
1994	5
1995	6
1996	2
1997	2
1998	1
1999	1
2000	1
2001	1
2002	2
2003	4
2004	1
2005	1
2006	2
2007	1
2009	1
2010	2
2011	3
2012	3
2013	1
2014	2
2015	3
2017	2
2018	1
2019	3
2020	1
2021	1
2022	4
2023	1
2024	1
2025	2

Applicants with the most clearances

Product code EGS

Applicants holding the most 510(k) clearances under product code EGS
Applicant	Clearances
Nakanishi Inc.	5
Saeshin Precision Co., Ltd.	5
Micro-Mega Societe Anonyme	4
Angstrom Mfg., Inc.	2
Aseptico, Inc.	2
Bvr Aero Precision Corp.	2
Handpiece Headquarters	2
Kerr Corporation (Danbury)	2
Midwest	2
Nsk Nakanishi, Inc.	2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 90 companies shown, in name order