Bone Screw Non-Sterilization Bulk
by OSSTEM IMPLANT Co., Ltd. 11 variants
Ref BSCH2016NB
Active
CE MDR 510(k)
Valid until
Not listed
FDA recalls
None foundTrust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number88000406OBNSML 08800040644224 | Date26 Feb 2026 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK251569 | Date13 Aug 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 24 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- United States
- European Union
Specification
- Device Name
- OssBuilder System (Non-Sterile)
- Model / Reference
- BSCH2016NB
- Primary DI / UDI-DI
- 08800040644224
- Basic UDI-DI
- 88000406OBNSML
- EMDN Code
- P01020101 Dental implants
- Device Class
- Class IIb
- EU market of registration
- Czechia
Manufacturer details
- EUDAMED SRN
- KR-MF-000020006
- Authorised representative
- Obelis s.a. BE-AR-000000106
Other devices from Osstem Implant Co., Ltd
Properties
Other properties (12)
- Sterile: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No