ORAMAGICRX ORAL WOUND RINSE— 510(k) K024180

Name: FDA 510(k) clearance K024180
Creator: U.S. Food and Drug Administration
Published: 2003-03-14

Substantially Equivalent

Mpm Medical., Inc.

FDA 510(k) clearance K024180 for ORAMAGICRX ORAL WOUND RINSE, Substantially Equivalent on 2003-03-14. Applicant: Mpm Medical., Inc.. Device class: Unclassified.

Clearance details

Applicant: Mpm Medical., Inc.
Product code: Code OLR
Device class: Unclassified
Advisory panel: Unknown
Date received: 2002-12-18
Decision date: 2003-03-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Belleville, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code OLR

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K260120 — NaturaJel Oral Wound Care Kit2026-08-05
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

More clearances from Mpm Medical., Inc.

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K060340 — ORAMAGIC PLUS ORAL WOUND RINSE2006-05-10
K020540 — REGENECARE WOUND GEL2002-11-01
K992074 — MPM REGENECARE WOUND GEL1999-12-23
K962160 — MPM HYDROGEL DRESSING (NON-STERILE)1996-06-26
K952276 — MPM HYDROGEL DRESSING1995-06-30

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.