Device 300419 Strip— 510(k) K260364
Substantially EquivalentGeistlich Pharma AG
FDA 510(k) clearance K260364 for Device 300419 Strip, Substantially Equivalent on 2026-06-02. Applicant: Geistlich Pharma AG. Device class: 2.
Clearance details
- Applicant
- Geistlich Pharma AG
- Product code
- Code MQV
- Device class
- Class 2
- Regulation
- 21 CFR 888.3045
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wolhusen, CH
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More clearances from Geistlich Pharma AG
view allAdverse events under product code MQV
product code MQV- Death
- 6
- Injury
- 435
- Total
- 441
Source: openFDA MAUDE database, through . 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.