Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Point Robotics MedTech with 5 510(k) clearances. The most recent is a 510(k) clearance dated Feb 20, 2026: “POINT” Kinguide Agile Hybrid Navigation System; DRF Accessories Set.
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.
| Feb 20, 2026 | “POINT” Kinguide Agile Hybrid Navigation System; DRF Accessories SetK252989 · OLO | 510(k) clearances |
| Jan 23, 2026 | POINT Kinguide Agile Robotic Arm Surgical Stereotactic SystemK252755 · OLO | 510(k) clearances |
| Jul 24, 2024 | “POINT” Kinguide Agile Hybrid Navigation System (PSHF01-000)K241130 · OLO | 510(k) clearances |
| Jul 17, 2023 | “POINT” Kinguide Agile Hybrid Navigation SystemK230087 · OLO | 510(k) clearances |
| Aug 9, 2022 | “POINT” Kinguide Robotic-Assisted Surgical SystemK220241 · OLO | 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
