Activator Methods EZIV Purple
by Activator Methods International Ltd.
Activator Methods EZIV Purple is a joint/spinal manipulator (FDA unclassified; FDA product code LXM, Manipulator, Plunger-Like Joint) made by Activator Methods International Ltd., cleared under FDA 510(k) K003185 on 20 Mar 2001 and listed in FDA GUDID since 16 Oct 2020 (UDI-DI 00850021303082), active as of 23 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 | Number00850021303082 | Date16 Oct 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK003185 | Date20 Mar 2001 | StatusActive |
Official records
- AccessGUDID record 00850021303082
- FDA 510(k) database K003185
Across registries
- FDA 510(k) K003185 decided 20 Mar 2001 Active
- FDA GUDID UDI-DI 00850021303082 listed 16 Oct 2020 Listed
Timeline
- Cleared FDA 510(k) K003185
- Listed FDA GUDID 00850021303082
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Activator Methods
- Generic name
- Joint/spinal manipulator, mechanical
- Model / reference
- EZIV Purple
- Primary DI / UDI-DI
- 00850021303082
- 510(k) Number
- FDA product code
- LXM
- GMDN term
- Joint/spinal manipulator, mechanical
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
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