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

Device, Jaw Tracking, For Monitoring Jaw Positions

21 CFR 872.2060 / Dental
FDA source (opens on fda.gov)

NFS is the FDA product code for Device, Jaw Tracking, For Monitoring Jaw Positions, a class I device type, regulated under 21 CFR 872.2060. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
NFS
Device name
Device, Jaw Tracking, For Monitoring Jaw Positions
Regulation
21 CFR 872.2060
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
2
Ingested recalls
0

Clearances, product code NFS

By decision year
2 clearances under product code NFS with a decision year between 1984 and 1995, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NFS by decision year
YearClearances
19841
19951

Applicants with the most clearances

Product code NFS
Applicants holding the most 510(k) clearances under product code NFS
ApplicantClearances
Bio-Research Associates, Inc.1
Siemens Medical Solutions USA, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 16 companies shown, in name order