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

Curette, Periodontic

21 CFR 872.4565 / Dental
FDA source (opens on fda.gov)

EMS is the FDA product code for Curette, Periodontic, a class I device type, regulated under 21 CFR 872.4565. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EMS
Device name
Curette, Periodontic
Regulation
21 CFR 872.4565
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
7
Ingested recalls
0

Clearances, product code EMS

By decision year
7 clearances under product code EMS with a decision year between 1982 and 1994, 1982 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code EMS by decision year
YearClearances
19822
19842
19872
19941

Applicants with the most clearances

Product code EMS
Applicants holding the most 510(k) clearances under product code EMS
ApplicantClearances
Military Engineering, Inc.2
Miltex, Inc.1
Minnesota Prophy Power, Inc.1
Pacific Dental Corp.1
Premier Dental Products Co1
Venture Technology, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 90 companies shown, in name order