FDA 510(k) Applications Submitted by Relign Corporation, Subsidiary of Zimmer Biomet

FDA 510(k) Number Submission Date Device Name Applicant
K241008 04/12/2024 Tricera Arthroscopic System; Tricera Controller (R-10001); Tricera Handpiece, Autoclavable (R-10023); Veriflow (R-10003); Exoflow (R-10017); 3-in-1 Shaver 4.2mm (R-10008); 3-in-1 Shaver 5.0mm (R-10014); Dynablator (R-10005); Standard Burr 5.0mm (R-10021) Relign Corporation, Subsidiary of Zimmer Biomet


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