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

Ultraviolet Lamp Products

21 CFR 878.4635 / General, Plastic Surgery
FDA source (opens on fda.gov)

SGZ is the FDA product code for Ultraviolet Lamp Products, a class II device type, regulated under 21 CFR 878.4635. FDA's definition for this code reads: "An ultraviolet lamp product intended to stimulate the production of Vitamin D". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
SGZ
Device name
Ultraviolet Lamp Products
FDA definition
An ultraviolet lamp product intended to stimulate the production of Vitamin D
Regulation
21 CFR 878.4635
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code SGZ

By decision year
1 clearance under product code SGZ with a decision year between 2026 and 2026, 2026 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code SGZ by decision year
YearClearances
20261

Applicants with the most clearances

Product code SGZ
Applicants holding the most 510(k) clearances under product code SGZ
ApplicantClearances
Solius Labs, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code