Ls Series Linear Stapler and Reloads, Clc Series Curved Linear Cutter and Reloads, Lc Series Linear Cutter and Reloads
K141367 is the FDA 510(k) clearance record for LS SERIES LINEAR STAPLER AND RELOADS, CLC SERIES CURVED LINEAR CUTTER AND RELOADS, LC SERIES LINEAR CUTTER AND RELOADS, a class II device, cleared for Touchstone International Medical Science Co., Ltd. on under FDA product code GDW (Staple, Implantable). FDA records list 2 510(k) clearances for Touchstone International Medical Science Co., Ltd., from to . As of , FDA records show no recalls naming K141367.
Clearance record
- Decision date
- Received
- (63 days to decision)
- Product code
- GDW Staple, Implantable
- Regulation
- 21 CFR 878.4750
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- Touchstone International Medical Science Co., Ltd. 21a Science Plz., Intrenational Science Park #1355, Suzhou, Jiangsu, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code GDW
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 1 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 1 |
| May 2026 | 1 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 1 |
| 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.
