JFBClass II

Table, Physical Therapy, Multi Function

21 CFR 890.5880 / Physical Medicine

JFB is the FDA product code for Table, Physical Therapy, Multi Function, a class II device type, regulated under 21 CFR 890.5880. As of 2026-09-10, FDA records hold 66 510(k) clearances under this code, the most recent dated 2025-07-11, and no recalls.

Classification record

Product code: JFB
Device name: Table, Physical Therapy, Multi Function
Regulation: 21 CFR 890.5880
Device class: Class II
Review panel: Physical Medicine
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 66
Ingested recalls: 0

Clearances, product code JFB

By decision year

66 clearances under product code JFB with a decision year between 1982 and 2025, 1987 the highest year at 7.

Show the numbers

510(k) clearances under FDA product code JFB by decision year
Year	Clearances
1982	1
1983	4
1984	2
1985	1
1986	3
1987	7
1988	4
1989	1
1990	3
1991	2
1992	2
1993	3
1994	2
1995	2
1997	1
1998	2
2000	2
2001	1
2003	1
2004	2
2006	2
2007	1
2008	1
2010	2
2011	2
2012	2
2014	1
2016	1
2021	2
2022	1
2024	2
2025	3

Applicants with the most clearances

Product code JFB

Applicants holding the most 510(k) clearances under product code JFB
Applicant	Clearances
Ceragem Co., Ltd.	7
Slenderizers Equipment Mfg., Inc.	7
Nuga Medical Co Ltd	3
Ceragem International, Inc.	2
Chattanooga Group, Inc.	2
Hill Laboratories	2
Inarex Corporation	2
Migun Medical Instrument Co., Ltd.	2
TJN Manufacturing,Inc.	2
Tri W-G, Inc.	2

Companies listing this code with FDA

Companies whose registered establishments list this code