K903009Substantially Equivalent
Argenco III
Argen Precious Metals, Inc., San Diego CA / Traditional, Substantially Equivalent
K903009 is the FDA 510(k) clearance record for ARGENCO III, a class II device, cleared for Argen Precious Metals, Inc. on under FDA product code EJS (Alloy, Other Noble Metal). FDA records list 217 510(k) clearances for Argen Precious Metals, Inc., from to . As of , FDA records show no recalls naming K903009.
Clearance record
- Decision date
- Received
- (35 days to decision)
- Product code
- EJS Alloy, Other Noble Metal
- Regulation
- 21 CFR 872.3060
- Device class
- Class II
- Review panel
- Dental
- Applicant
- Argen Precious Metals, Inc. 8380 Miralani Dr., San Diego CA
- Third party review
- No
Clearances, product code EJS
Trailing 12 monthsFDA records hold no clearances under product code EJS in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| 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 |
| November 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.
