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» FDA gives nod to Orthocell’s 510(k) for nerve repair product
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FDA gives nod to Orthocell’s 510(k) for nerve repair product
April 9, 2025
By
Tamra Sami
The U.S. FDA has cleared regenerative medicine company Orthocell Ltd.’s 510(k) for its nerve repair product, Remplir, paving the way to begin commercial operations in the $1.6 billion U.S. nerve repair market.
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