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

Injector, Capsular Tension Ring

21 CFR 886.4300 / Ophthalmic
FDA source (opens on fda.gov)

NCE is the FDA product code for Injector, Capsular Tension Ring, a class I device type, regulated under 21 CFR 886.4300. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
NCE
Device name
Injector, Capsular Tension Ring
Regulation
21 CFR 886.4300
Device class
Class I
Review panel
Ophthalmic
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
3
Ingested recalls
0

Clearances, product code NCE

By decision year
3 clearances under product code NCE with a decision year between 2000 and 2004, 2000 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NCE by decision year
YearClearances
20001
20011
20041

Applicants with the most clearances

Product code NCE
Applicants holding the most 510(k) clearances under product code NCE
ApplicantClearances
Duckworth & Kent, Ltd.1
Geuder AG1
Ophtec USA, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code