Inqu Paste Mix Plus
510(k) K103799
Inqu Paste Mix Plus is a Class II device made by Isto Technologies, Inc., cleared under FDA 510(k) K103799 on 29 Aug 2011, 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 | FDA 510(k)SESE | NumberK103799 | Date29 Aug 2011 | StatusActive |
Official records
- FDA 510(k) database K103799
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MQV
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3045
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K103799
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| InQu Paste Mix Plus 1.25cc IQSP-PP-101 | IQSP-PP-101 / IQSP-PP-101 | M896IQSPPP1010 | — | On the market |
| InQu Paste Mix Plus 10cc IQSP-PP-110 | IQSP-PP-110 / IQSP-PP-110 | M896IQSPPP1100 | — | On the market |
| InQu Paste Mix Plus 2.5cc IQSP-PP-102 | IQSP-PP-102 / IQSP-PP-102 | M896IQSPPP1020 | — | On the market |
| InQu Paste Mix Plus 5cc IQSP-PP-105 | IQSP-PP-105 / IQSP-PP-105 | M896IQSPPP1050 | — | On the market |
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