JDYClass I

Evacuator, Vapor, Cement Monomer

21 CFR 888.4220 / Orthopedic

JDY is the FDA product code for Evacuator, Vapor, Cement Monomer, a class I device type, regulated under 21 CFR 888.4220. As of 2026-09-10, FDA records hold 8 510(k) clearances under this code, the most recent dated 1991-01-04, and one recall.

Classification record

Product code: JDY
Device name: Evacuator, Vapor, Cement Monomer
Regulation: 21 CFR 888.4220
Device class: Class I
Review panel: Orthopedic
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 8
Ingested recalls: 1

Clearances, product code JDY

By decision year

8 clearances under product code JDY with a decision year between 1976 and 1991, 1976 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code JDY by decision year
Year	Clearances
1976	1
1977	1
1978	1
1979	1
1981	1
1986	1
1990	1
1991	1

Applicants with the most clearances

Product code JDY

Applicants holding the most 510(k) clearances under product code JDY
Applicant	Clearances
Howmedica Corp.	2
Arbor Technologies, Inc.	1
Hollister, Inc.	1
Lifestream Int'L, Inc.	1
Medishield, Inc.	1
Stackhouse Assoc.	1
Walgen Medical Innoventions	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 17 companies shown, in name order