MESHEET— 510(k) K233544

Name: FDA 510(k) clearance K233544
Creator: U.S. Food and Drug Administration
Published: 2024-02-22

Substantially Equivalent

Dentis Co., Ltd.

FDA 510(k) clearance K233544 for MESHEET, Substantially Equivalent on 2024-02-22. Applicant: Dentis Co., Ltd.. Device class: 2.

Clearance details

Applicant: Dentis Co., Ltd.
Product code: Code NXC
Device class: Class 2
Regulation: 21 CFR 872.5470
Advisory panel: Dental
Date received: 2023-11-03
Decision date: 2024-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Daegu, KR

Download summary PDF View on FDA.gov ↗

Recent devices under product code NXC

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K260527 — FACE4D Aligner2026-07-02
K260788 — Smylio Aligners2026-05-08
K260722 — SureSmile Aligner (ASSY500020)2026-04-15
K253282 — ZSmile System2026-02-03
K251454 — Clear Aligner (SCF-3348)2026-01-07

More clearances from Dentis Co., Ltd.

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K253493 — Dentis SQ-SL AXEL Fixture2026-03-04
K241065 — ChecQ (AC100)2025-03-21
K233921 — Luvis Chair (LC700C)2024-09-06
K241063 — s-Clean ScanHealing Abutment2024-07-25
K240511 — Dentis s-Clean SQ-SL Fixture2024-05-20

Adverse events under product code NXC

product code NXC

Injury: 15,206
Malfunction: 2,576
Other: 9
Total: 17,791

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.