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

Attachment, Eyepiece, For Insertion Of Prescription Lens

21 CFR 876.1500 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FDZ is the FDA product code for Attachment, Eyepiece, For Insertion Of Prescription Lens, a class I device type, regulated under 21 CFR 876.1500. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FDZ
Device name
Attachment, Eyepiece, For Insertion Of Prescription Lens
Regulation
21 CFR 876.1500
Device class
Class I
Review panel
Gastroenterology, Urology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code FDZ

By decision year
2 clearances under product code FDZ with a decision year between 1986 and 1990, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FDZ by decision year
YearClearances
19861
19901

Applicants with the most clearances

Product code FDZ
Applicants holding the most 510(k) clearances under product code FDZ
ApplicantClearances
Exel Intl.1
Teleflexmedical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code