510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
JETClass I

Pick, Massaging

21 CFR 872.6650 / Dental
FDA source (opens on fda.gov)

JET is the FDA product code for Pick, Massaging, a class I device type, regulated under 21 CFR 872.6650. As of , FDA records hold 15 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
JET
Device name
Pick, Massaging
Regulation
21 CFR 872.6650
Device class
Class I
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
15
Ingested recalls
2

Clearances, product code JET

By decision year
15 clearances under product code JET with a decision year between 1982 and 1996, 1988 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code JET by decision year
YearClearances
19822
19831
19841
19851
19861
19883
19892
19911
19931
19951
19961

Applicants with the most clearances

Product code JET
Applicants holding the most 510(k) clearances under product code JET
ApplicantClearances
Arizona Implant Dentistry1
Burn-Henderson Partnership1
Coopercare, Inc.1
Dental Concepts, LLC1
Dentek Corp.1
L.A.K. Ent., Inc.1
Martin A. Hass, D.D.S.1
Moyco Industries, Inc.1
Oral-B Laboratories1
Richard G. Deniro1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 123 companies shown, in name order