Stripper MXL3-50
by Origio Inc.
Stripper MXL3-50 is a Class II device made by Origio Inc., cleared under FDA 510(k) K993699 on 16 May 2000 and listed in FDA GUDID since 22 Aug 2016 (UDI-DI 20888937906282), 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 | Number20888937906282 | Date22 Aug 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK993699 | Date16 May 2000 | StatusActive |
Official records
- AccessGUDID record 20888937906282
- FDA 510(k) database K993699
Across registries
- FDA 510(k) K993699 decided 16 May 2000 Active
- FDA GUDID UDI-DI 20888937906282 listed 22 Aug 2016 Listed
Timeline
- Cleared FDA 510(k) K993699
- Listed FDA GUDID 20888937906282
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Stripper
- Generic name
- Assisted reproduction microtool
- Model / reference
- MXL3-50
- Primary DI / UDI-DI
- 20888937906282
- 510(k) Number
- FDA product code
- MQH
- GMDN term
- Assisted reproduction microtool
- Device class
- Class II
- Regulation number
- 884.6130
- GUDID distribution status
- In Commercial Distribution
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