Lantern 502000-02
Active
510(k)
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00810832032489 | Date12 Dec 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK242616 | Date3 Oct 2024 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Lantern
- Generic name
- Orthopaedic stereotactic surgery system
- Model / Ref / Catalog
- 502000-02
- Primary DI / UDI-DI
- 00810832032489
- 510(k) Number
- FDA product code
- ONN
- GMDN term
- Orthopaedic stereotactic surgery system
- Device class
- Class II
- Regulation number
- 882.4560
- GUDID distribution status
- In Commercial Distribution
Other devices from Orthalign, Inc.
Properties
Other properties (9)
- Sterilise before use: No
- Implantable: No
- Contains latex: No
- Over-the-counter: No
- Convenience kit: No
- Combination product: No
- HCT/P: No
- Premarket exempt: No
- Manufacturing date: No