Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Renovis Surgical Technologies with 23 510(k) clearances. The most recent is a 510(k) clearance dated Jun 20, 2019: Renovis A200 PS Knee System as part of the Renovis A200 Knee System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 20, 2019 | Renovis A200 PS Knee System as part of the Renovis A200 Knee SystemK190122 · JWH | 510(k) clearances |
| Dec 7, 2018 | Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) SystemK182007 · OVD | 510(k) clearances |
| Sep 11, 2018 | Renovis S180 Lateral Lumbar Interbody Fusion SystemK181655 · MAX | 510(k) clearances |
| Jun 14, 2018 | S128 Anterior Lumbar Interbody Fusion (ALIF) SystemK180502 · OVD | 510(k) clearances |
| Nov 16, 2017 | Renovis Surgical Hip Replacement SystemK171543 · OQG | 510(k) clearances |
| Aug 8, 2017 | Renovis S141 Lumbar Interbody Fusion SystemK170888 · MAX | 510(k) clearances |
| Mar 16, 2016 | Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) SystemK153250 · OVE | 510(k) clearances |
| Sep 25, 2015 | Renovis Anterior Cervical Plate SystemK152193 · KWQ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
