Suzhou Endophix Co., Ltd.
Suzhou Endophix Co., Ltd. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 3, 2024.
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Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K232941 | Megaloop Button System | May 3, 2024 |
| K232725 | Javelot Ti Suture Anchor, Javelot Ti-D Suture Anchor | Nov 2, 2023 |
| K231002 | Javelot PK-S suture anchor, Javelot PK-S suture anchor (Knotless), Javelot PK-P suture anchor, Javel | Jun 7, 2023 |
| K230874 | Syntheface PEEK Interference Screw, Syntheface PEEK Screw Sheath | May 23, 2023 |