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

Band, Material, Orthodontic

21 CFR 872.5410 / Dental
FDA source (opens on fda.gov)

DYO is the FDA product code for Band, Material, Orthodontic, a class I device type, regulated under 21 CFR 872.5410. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DYO
Device name
Band, Material, Orthodontic
Regulation
21 CFR 872.5410
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
3
Ingested recalls
0

Clearances, product code DYO

By decision year
3 clearances under product code DYO with a decision year between 1985 and 1994, 1985 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DYO by decision year
YearClearances
19851
19931
19941

Applicants with the most clearances

Product code DYO
Applicants holding the most 510(k) clearances under product code DYO
ApplicantClearances
Dentauraum, Inc.1
Echo Ultrasound1
Ortho Organizers Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 46 companies shown, in name order