K821054 is the FDA 510(k) clearance record for TOTAL, cleared for Allergan, Inc. on under FDA product code HPX (Lens, Contact (Polymethylmethacrylate)). FDA records list 39 510(k) clearances for Allergan, Inc., from to . As of , FDA records show no recalls naming K821054.
Clearance record
- Decision date
- Received
- (28 days to decision)
- Product code
- HPX Lens, Contact (Polymethylmethacrylate)
- Device class
- Unclassified
- Review panel
- Unknown
- Applicant
- Allergan, Inc. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
Clearances, product code HPX
Trailing 12 monthsFDA records hold no clearances under product code HPX in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
