Incore Co., Ltd.
FDA Regulatory Profile
Incore Co., Ltd. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 19, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K232216 | Hemoblock_S (Prescription); Hemoblock_S (OTC) | April 19, 2024 |
| K221054 | CORE-INJECTOR | December 21, 2022 |
| K220846 | CORE-SNARE | November 21, 2022 |
| K220081 | CORE-SPORT | September 28, 2022 |
| K213338 | CORE-CLIP | June 23, 2022 |
| K211148 | CORE-Trocar | June 21, 2022 |