FDA 510(k) Applications Submitted by WONTECH Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K183156 | 11/15/2018 | V-Laser | WONTECH Co., Ltd. |
| K241527 | 05/30/2024 | Pastelle Pro | Wontech Co., Ltd. |
| K250165 | 01/21/2025 | Pastelle | WONTECH Co., Ltd. |
| K251288 | 04/25/2025 | Veincare | WONTECH CO., LTD. |
| K241930 | 07/01/2024 | Veincare | Wontech Co., Ltd. |
| K243957 | 12/23/2024 | PICOALEX | WONTECH CO., LTD. |
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