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

Ring, Ophthalmic (Flieringa)

21 CFR 886.4350 / Ophthalmic
FDA source (opens on fda.gov)

HNH is the FDA product code for Ring, Ophthalmic (Flieringa), a class I device type, regulated under 21 CFR 886.4350. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HNH
Device name
Ring, Ophthalmic (Flieringa)
Regulation
21 CFR 886.4350
Device class
Class I
Review panel
Ophthalmic
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 HNH

By decision year
7 clearances under product code HNH with a decision year between 1984 and 1991, 1991 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code HNH by decision year
YearClearances
19841
19851
19861
19901
19913

Applicants with the most clearances

Product code HNH
Applicants holding the most 510(k) clearances under product code HNH
ApplicantClearances
Ocular Instruments, Inc.5
Ameritek, Inc.1
Miami Eye Technology, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 88 companies shown, in name order