Prosidyan, Inc.
Philedelphia, PA, US
Prosidyan, Inc. appears in FDA device records in Philedelphia, PA. FDA records list 12 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Prosidyan, Inc. between 2014 and 2025. The busiest year on record is 2014, with 2. The most recent is 2025, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2014 | 2 |
| 2015 | 2 |
| 2017 | 2 |
| 2018 | 2 |
| 2022 | 1 |
| 2024 | 1 |
| 2025 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K253147 | FIBERGRAFT™ BG Putty GPS Bone Graft Substitute FIBERGRAFT™ BG Putty Bone Graft Substitute FIBERGRAFT™ AERIDYAN™ Matrix Bone Graft Substitute FIBERGRAFT™ BG Matrix Bone Graft Substitute | MQV | Substantially Equivalent | |
| K251648 | GPS Advanced; GPS Advanced Cannula | FMF | Substantially Equivalent | |
| K241426 | GPS Advanced; 5 cc GPS Advanced Cannula | FMF | Substantially Equivalent | |
| K213803 | FIBERGRAFT Aeridyan Matrix Bone Graft Substitute | MQV | Substantially Equivalent | |
| K182670 | FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute | MQV | Substantially Equivalent | |
| K180080 | FIBERGRAFT BG Matrix Bone Graft Substitute | MQV | Substantially Equivalent | |
| K171284 | FIBERGRAFT BG Matrix Bone Graft Substitute | MQV | Substantially Equivalent | |
| K170306 | FIBERGRAFT BG Putty Bone Graft Substitute | MQV | Substantially Equivalent | |
| K151154 | FIBERGRAFT BG Morsels | MQV | Substantially Equivalent | |
| K143533 | FIBERGRAFT BG PUTTY BONE GRAFT SUBSTITUTE | MQV | Substantially Equivalent | |
| K141956 | FIBERGRAFT BG MORSELS | MQV | Substantially Equivalent | |
| K132805 | BG MORSELS | MQV | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
