Geliperm Granules
FDA 510(k) K823225 · Geistlich-Pharma
510(k) numberK823225
Submission
- Device name
- Geliperm Granules
- Applicant
- Geistlich-Pharma
Mchenry, IL, US - Received
- October 29, 1982
- Decision date
- August 12, 1983
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FRO – Dressing, Wound, Drug
- Device class
- Unclassified
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| K251556 | Device 300423 GranulesMQV · Traditional | 07/17/2025SE |
| K251786 | Geistlich Bio-Oss®; Geistlich Bio-Oss Pen®NPM · Special | 07/11/2025SE |
| K251613 | SwissGraft XNPM · Special | 06/26/2025SE |
| K250833 | SwissMembrane X; SwissMembrane X SocketNPL · Special | 04/15/2025SE |
| K242510 | Geistlich Bio-Flow®NPM · Traditional | 03/07/2025SE |
Questions and answers
When was Geliperm Granules cleared by the FDA?
Geliperm Granules (K823225) received a 510(k) decision of Substantially Equivalent on August 12, 1983, 287 days after the submission was received.
What is the product code of K823225?
The FDA product code is FRO – Dressing, Wound, Drug, a Unclassified device.