510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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JYGClass I

Curette, Ear

21 CFR 874.4420 / Ear, Nose, Throat
FDA source (opens on fda.gov)

JYG is the FDA product code for Curette, Ear, a class I device type, regulated under 21 CFR 874.4420. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
JYG
Device name
Curette, Ear
Regulation
21 CFR 874.4420
Device class
Class I
Review panel
Ear, Nose, Throat
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
7
Ingested recalls
1

Clearances, product code JYG

By decision year
7 clearances under product code JYG with a decision year between 1982 and 1993, 1982 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JYG by decision year
YearClearances
19822
19831
19842
19851
19931

Applicants with the most clearances

Product code JYG
Applicants holding the most 510(k) clearances under product code JYG
ApplicantClearances
Kelleher Corp.2
Treace Medical, Inc.2
Bionix, LLC1
Ear Tech, Inc.1
Premier Dental Products Co1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 144 companies shown, in name order