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

Accessories, Implant, Dental, Endosseous

21 CFR 872.3980 / Dental
FDA source (opens on fda.gov)

NDP is the FDA product code for Accessories, Implant, Dental, Endosseous, a class I device type, regulated under 21 CFR 872.3980. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and 57 recalls.

Classification record

Product code
NDP
Device name
Accessories, Implant, Dental, Endosseous
Regulation
21 CFR 872.3980
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
57

Clearances, product code NDP

By decision year
4 clearances under product code NDP with a decision year between 2007 and 2020, 2007 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NDP by decision year
YearClearances
20071
20171
20191
20201

Applicants with the most clearances

Product code NDP
Applicants holding the most 510(k) clearances under product code NDP
ApplicantClearances
Dentsply Sirona Inc3
Thommen Medical AG1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 499 companies shown, in name order