Aeon-C
by Dio Medical Co., Ltd. 508 variants
Aeon-C (CSA.12160708) is a Class II device made by Dio Medical Co., Ltd., listed in FDA GUDID since 29 Dec 2019 (UDI-DI 08800039834865), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08800039834865 | Date29 Dec 2019 | StatusListed |
Official records
- AccessGUDID record 08800039834865
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Spinal fixation plate, non-bioabsorbable
- Model / Ref / Catalog
- A, CSA.12160708
- Primary DI / UDI-DI
- 08800039834865
- FDA product code
- OVE
- GMDN term
- Spinal fixation plate, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3080
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- MRI safety
- MR Unsafe
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