JOJClass II

Indicator, Physical/Chemical Sterilization Process

21 CFR 880.2800 / General Hospital

JOJ is the FDA product code for Indicator, Physical/Chemical Sterilization Process, a class II device type, regulated under 21 CFR 880.2800. As of 2026-09-10, FDA records hold 264 510(k) clearances under this code, the most recent dated 2026-02-20, and 24 recalls.

Classification record

Product code: JOJ
Device name: Indicator, Physical/Chemical Sterilization Process
Regulation: 21 CFR 880.2800
Device class: Class II
Review panel: General Hospital
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 265
Ingested recalls: 24

Clearances, product code JOJ

By decision year

265 clearances under product code JOJ with a decision year between 1976 and 2026, 2011 the highest year at 13.

Show the numbers

510(k) clearances under FDA product code JOJ by decision year
Year	Clearances
1976	1
1977	3
1978	1
1980	7
1981	6
1982	6
1983	3
1984	3
1985	3
1988	3
1989	10
1990	3
1991	1
1993	3
1994	5
1995	4
1996	4
1997	5
1998	10
1999	9
2000	7
2001	3
2002	8
2003	5
2004	5
2005	3
2006	4
2007	8
2008	9
2009	7
2010	6
2011	13
2012	7
2013	6
2014	6
2015	8
2016	4
2017	7
2018	5
2019	12
2020	7
2021	4
2022	8
2023	4
2024	11
2025	6
2026	2

Applicants with the most clearances

Product code JOJ

Applicants holding the most 510(k) clearances under product code JOJ
Applicant	Clearances
STERIS Corporation	42
3M Company	22
Spsmedical Supply Corp.	17
Sybron Dental Specialties, Inc.	16
Steritec Products Mfg. Co., Inc.	16
Serim Research Corp.	12
Steritec Products, Inc.	12
Propper Mfg Co Inc	11
Advanced Sterilization Products	8
Dana Products, Inc.	6

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 118 companies shown, in name order