Dannik Titanium Ligation Clip— 510(k) K192711

Name: FDA 510(k) clearance K192711
Creator: U.S. Food and Drug Administration
Published: 2019-12-20

Substantially Equivalent

Dannik

FDA 510(k) clearance K192711 for Dannik Titanium Ligation Clip, Substantially Equivalent on 2019-12-20. Applicant: Dannik. Device class: 2.

Clearance details

Applicant: Dannik
Product code: Code FZP
Device class: Class 2
Regulation: 21 CFR 878.4300
Advisory panel: General, Plastic Surgery
Date received: 2019-09-27
Decision date: 2019-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Winter Park, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FZP

view all

K254231 — Inno-Hook Disposable Clip Appliers (Ligating Clips) and Inno-Hook Ligating Clips2026-07-20
K253781 — InnoClip Clip Applier2025-12-22
K253903 — InnoClip Disposable Clip Applier2025-12-22
K250643 — Disposable Polymer Ligation Clips2025-11-20
K251054 — Hem-o-lok PurplePlus Large Polymer Ligating Clips2025-07-03

More clearances from Dannik

view all

Adverse events under product code FZP

product code FZP

Death: 11
Injury: 726
Malfunction: 10,830
Other: 1
Total: 11,568

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.