Apyx Medical Corporation Receives FDA 510(k) Clearance for the Use of Renuvion to Improve Appearance of Lax (Loose) Skin
The Renuvion APR Handpieces are now indicated for use in subcutaneous dermatological and aesthetic procedures to improve the…
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19 Jul 22
The Renuvion APR Handpieces are now indicated for use in subcutaneous dermatological and aesthetic procedures to improve the…
11 Jul 22
The Agreement covers the sales & marketing of LASEROPTEK's expanding line of FDA cleared aesthetic laser systems to…
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STENTiT, Vivolta and Corbion announced their first collaboration to develop a regenerative stent for clinical use, with an…
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Medios AI is not US FDA approved and not available in the US
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Testing in accordance with ISO 18562 and ISO 10993 standards conducted by five certified, independent testing laboratories in…
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With the IDE approval, the company is now allowed to study its investigational Flash treatment modality in the…
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Incorporating the SSS shoulder device with BioMech Lab will provide automated functional mobility data collecting and analysis ability…