Secret Line up (FC1938E80 FC1950E90 FC1960E100 FC1970E120 FC1990E150 FC19100E150 FC19100E280 FC19100E420 FC2038E80 FC2050E90 FC2060E100 FC2070E120 FC2090E150 FC20100E170 FC2138G80 FC2150G90 FC2160G100 FC2170G120 FC2190G150 FC21100G170 FCL18100C160 FCL1938E80 FCL1950E90 FCL1960E100 FCL1970E120 FCL1990E150 FCL19100E160 FCL2138G80 FCL2150G90 FCL2160G100 FCL2170G120 FCL2190G150 FCL21100G160 FCRL1870C162 FCRL18100C185 FCRL1970E162 FCRL19100E185 FCHL1960E90 FCHL1970E120 FCHL19100E160 FCW1938
K242571 is the FDA 510(k) clearance record for Secret Line up (FC1938E80 FC1950E90 FC1960E100 FC1970E120 FC1990E150 FC19100E150 FC19100E280 FC19100E420 FC2038E80 FC2050E90 FC2060E100 FC2070E120 FC2090E150 FC20100E170 FC2138G80 FC2150G90 FC2160G100 FC2170G120 FC2190G150 FC21100G170 FCL18100C160 FCL1938E80 FCL1950E90 FCL1960E100 FCL1970E120 FCL1990E150 FCL19100E160 FCL2138G80 FCL2150G90 FCL2160G100 FCL2170G120 FCL2190G150 FCL21100G160 FCRL1870C162 FCRL18100C185 FCRL1970E162 FCRL19100E185 FCHL1960E90 FCHL1970E120 FCHL19100E160 FCW1938, a class II device, cleared for Hyundae Meditech Co., Ltd. on under FDA product code NEW (Suture, Surgical, Absorbable, Polydioxanone). FDA records list 2 510(k) clearances for Hyundae Meditech Co., Ltd., from to . As of , FDA records show no recalls naming K242571.
Clearance record
- Decision date
- Received
- (29 days to decision)
- Product code
- NEW Suture, Surgical, Absorbable, Polydioxanone
- Regulation
- 21 CFR 878.4840
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- Hyundae Meditech Co., Ltd. 80, Cheongjeong-Ro, Jijeong-Myeon, Wonju-Si, KR
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code NEW
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 1 |
| June 2026 | 1 |
| July 2026 | 1 |
| August 2026 | 1 |
| September 2026 | 1 |
| October 2026 | 0 |
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