Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Medical Metrics, Inc. with 5 510(k) clearances and 2 AI-enabled devices. The most recent is a 510(k) clearance dated Jul 7, 2023: Spine CAMP™ (1.1).
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.
| Jul 7, 2023 | Spine CAMP™ (1.1)K231668 · QIH | 510(k) clearances |
| Jul 7, 2023 | Spine CAMP (1.1)K231668 · Radiology | AI-enabled devices |
| Oct 18, 2022 | Spine CAMP™K221632 · QIH | 510(k) clearances |
| Oct 18, 2022 | Spine CAMPK221632 · Radiology | AI-enabled devices |
| Oct 11, 2002 | KIMAX QMAK022585 · LLZ | 510(k) clearances |
| Dec 7, 2001 | KIMAX REMOTE VIEWING STATIONK013098 · LLZ | 510(k) clearances |
| Feb 14, 2001 | KIMAX, MODEL 1024K010187 · JAA | 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
