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 14, 2026, FDA's public records list OrthoGrid Systems, Inc. with 4 510(k) clearances and 2 AI-enabled devices. The most recent is a 510(k) clearance dated May 29, 2026: OrthoGrid Hip AI® 4.0.
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.
| May 29, 2026 | OrthoGrid Hip AI® 4.0K260077 · QIH | 510(k) clearances |
| May 29, 2026 | OrthoGrid Hip AI® 4.0K260077 · Radiology | AI-enabled devices |
| Feb 18, 2021 | PhantomMSK HipK210136 · LLZ | 510(k) clearances |
| Dec 7, 2019 | PhantomMSK TraumaK192279 · LLZ | 510(k) clearances |
| Dec 7, 2019 | PhantomMSK TraumaK192279 · Radiology | AI-enabled devices |
| Feb 15, 2019 | PhantomMSKK182332 · LLZ | 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
