AONGEN DENTAL COLLAGEN MATRIX— 510(k) K112568

Name: FDA 510(k) clearance K112568
Creator: U.S. Food and Drug Administration
Published: 2012-03-01

Substantially Equivalent

Aeon Astron Europe B.V.

FDA 510(k) clearance K112568 for AONGEN DENTAL COLLAGEN MATRIX, Substantially Equivalent on 2012-03-01. Applicant: Aeon Astron Europe B.V.. Device class: Unclassified.

Clearance details

Applicant: Aeon Astron Europe B.V.
Product code: Code OLR
Device class: Unclassified
Advisory panel: Unknown
Date received: 2011-09-06
Decision date: 2012-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Leiden, NL

Download summary PDF View on FDA.gov ↗

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K251908 — Emanate Tray2026-07-29
K260126 — Curajel Oral Gel2026-06-15
K253816 — MuCover (proposed name) Oral Wound Dressing2026-05-21
K253758 — Dental Cone; Dental Sponge2025-12-18

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K173223 — ologen Collagen Matrix2018-03-02
K080868 — AONGEN COLLAGEN MATRIX2009-05-14

Adverse events under product code OLR

product code OLR

Death: 3
Total: 3

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.