FirmLabelled 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 K&J Consulting Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 29, 2025: IVA & AEON Cervical and Lumbar Cage 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.
| Aug 29, 2025 | IVA & AEON Cervical and Lumbar Cage SystemK250335 · ODP | 510(k) clearances |
| Dec 13, 2023 | FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone SystemK232877 · MRW | 510(k) clearances |
| Nov 27, 2023 | Statera-C™ Spinal SystemK233332 · NKG | 510(k) clearances |
| Oct 24, 2023 | Rexious Spinal Fixation System, Statera™ Spinal System, Statera-M™ Spinal SystemK232586 · NKB | 510(k) clearances |
| Jul 16, 2023 | FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, BALTEUM™ & BALTEUM-ONE™ Lumbar Plate System, and Osprey™ Anterior Cervical Plate SystemK231460 · KWQ | 510(k) clearances |
| Aug 27, 2021 | K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK CageK212038 · ODP | 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
