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
NFQClass I

Device, Dental Sonography, For Monitoring Jaw Sounds

21 CFR 872.2050 / Dental
FDA source (opens on fda.gov)

NFQ is the FDA product code for Device, Dental Sonography, For Monitoring Jaw Sounds, a class I device type, regulated under 21 CFR 872.2050. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
NFQ
Device name
Device, Dental Sonography, For Monitoring Jaw Sounds
Regulation
21 CFR 872.2050
Device class
Class I
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
4
Ingested recalls
0

Clearances, product code NFQ

By decision year
4 clearances under product code NFQ with a decision year between 1987 and 1997, 1991 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code NFQ by decision year
YearClearances
19871
19912
19971

Applicants with the most clearances

Product code NFQ
Applicants holding the most 510(k) clearances under product code NFQ
ApplicantClearances
Myo-Tronics, Inc.2
Arthrotek, Inc.1
Bioresearch1

Companies listing this code with FDA

Companies whose registered establishments list this code