SureMAX 1
by Additive Implants, Inc. 146 variants
SureMAX 1 is a Class I device made by Additive Implants, Inc., cleared under FDA 510(k) K182477 on 28 Jan 2019 and listed in FDA GUDID since 21 Feb 2019 (UDI-DI 00817662024363), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00817662024363 | Date21 Feb 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK182477 | Date28 Jan 2019 | StatusActive |
Official records
- AccessGUDID record 00817662024363
- FDA 510(k) database K182477
Across registries
- FDA 510(k) K182477 decided 28 Jan 2019 Active
- FDA GUDID UDI-DI 00817662024363 listed 21 Feb 2019 Listed
Timeline
- Cleared FDA 510(k) K182477
- Listed FDA GUDID 00817662024363
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- SureMAX
- Generic name
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Model / reference
- 1
- Primary DI / UDI-DI
- 00817662024363
- 510(k) Number
- FDA product code
- LXH
- GMDN term
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Angle — 7 degreeDepth — 14 MillimeterWidth — 16 MillimeterHeight — 4.5 Millimeter
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