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
MEFClass I

Ring, Teething, Non-Fluid Filled

21 CFR 872.5550 / Dental
FDA source (opens on fda.gov)

MEF is the FDA product code for Ring, Teething, Non-Fluid Filled, a class I device type, regulated under 21 CFR 872.5550. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
MEF
Device name
Ring, Teething, Non-Fluid Filled
Regulation
21 CFR 872.5550
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
1
Ingested recalls
1

Clearances, product code MEF

By decision year
1 clearance under product code MEF with a decision year between 2004 and 2004, 2004 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MEF by decision year
YearClearances
20041

Applicants with the most clearances

Product code MEF
Applicants holding the most 510(k) clearances under product code MEF
ApplicantClearances
Vibe 20001

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 83 companies shown, in name order