InQu Paste Mix Plus 1.25cc IQSP-PP-101
by Arteriocyte Medical Systems, Inc
InQu Paste Mix Plus 1.25cc IQSP-PP-101 is a Class II device made by Arteriocyte Medical Systems, Inc, cleared under FDA 510(k) K103799 on 29 Aug 2011 and listed in FDA GUDID since 1 Aug 2018 (UDI-DI M896IQSPPP1010), active as of 8 Nov 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 | NumberM896IQSPPP1010 | Date1 Aug 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK103799 | Date29 Aug 2011 | StatusActive |
Official records
- FDA 510(k) database K103799
Across registries
- FDA 510(k) K103799 decided 29 Aug 2011 Active
- FDA GUDID UDI-DI M896IQSPPP1010 listed 1 Aug 2018 Listed
Timeline
- Cleared FDA 510(k) K103799
- Listed FDA GUDID M896IQSPPP1010
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- InQu Paste Mix Plus 1.25cc
- Generic name
- Synthetic bone graft
- Model / Ref / Catalog
- IQSP-PP-101
- Primary DI / UDI-DI
- M896IQSPPP1010
- 510(k) Number
- FDA product code
- MQV
- GMDN term
- Synthetic bone graft
- Device class
- Class II
- Regulation number
- 888.3045
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Synthetic bone graft.