FDA 510(k) Applications Submitted by Orthorebirth Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K142090 | 08/01/2014 | REBOSSIS | ORTHOREBIRTH CO., LTD. |
| K170620 | 03/01/2017 | ReBOSSIS85 | ORTHOREBIRTH Co., Ltd. |
| K172573 | 08/28/2017 | ReBOSSIS85 | Orthorebirth Co., Ltd. |
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