INBODY
Analyzer, Body Composition
BIOSPACE CORPORATION LIMITED
The following data is part of a premarket notification filed by Biospace Corporation Limited with the FDA for Inbody.
Pre-market Notification Details
| Device ID | K110689 |
| 510k Number | K110689 |
| Device Name: | INBODY |
| Classification | Analyzer, Body Composition |
| Applicant | BIOSPACE CORPORATION LIMITED 8870 RAVELLO CT Naples, FL 34114 |
| Contact | Daniel Kamm |
| Correspondent | Daniel Kamm BIOSPACE CORPORATION LIMITED 8870 RAVELLO CT Naples, FL 34114 |
| Product Code | MNW |
| CFR Regulation Number | 870.2770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-03-15 |
| Decision Date | 2011-08-19 |
| Summary: | summary |
Trademark Results [INBODY]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INBODY 86918373 5546337 Live/Registered |
InBody Co., Ltd. 2016-02-24 |
 INBODY 85447575 4160606 Live/Registered |
INBODY CO., LTD. 2011-10-14 |
 INBODY 76165230 2815341 Dead/Cancelled |
BIOSPACE CO., LTD. 2000-11-13 |
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