# K&J Consulting Corp.

- Location (FDA's records): Lansdale, PA
- FDA decisions: 6 (2021–2025): 6 510(k) clearances
- Names in FDA's records: K&J Consulting Corp. (3); K&J Consulting Corporation (2); K&J Consulting (1)
- Product codes: ODP (2), KWQ (1), MRW (1), NKB (1), NKG (1)
- 510(k) review time since 2016: median 60 days, against 80 for FDA's reviews in the same codes and years (4 of 6 faster)
- Predicates its devices cite: 15 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Dio Medical Co., Ltd.: 7 (https://510kreport.com/company/dio-medical)
- Globus Medical, Inc.: 4 (https://510kreport.com/company/globus-medical)
- Camber Spine Technologies: 2 (https://510kreport.com/company/camber-spine-technologies)

## Its most-cited devices
- K212038: K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage (2021), cited by 1
- K232877: FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System (2023), cited by 1

## Recent decisions
- K250335: IVA & AEON Cervical and Lumbar Cage System (Aug 29, 2025)
- K232877: FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System (Dec 13, 2023)
- K233332: Statera-C™ Spinal System (Nov 27, 2023)
- K232586: Rexious Spinal Fixation System, Statera™ Spinal System, Statera-M™ Spinal System (Oct 24, 2023)
- K231460: FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, BALTEUM™ & BALTEUM-ONE™ Lumbar Plate System, and Osprey™ Anterior Cervical Plate System (Jul 16, 2023)
- K212038: K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage (Aug 27, 2021)

Source page: https://510kreport.com/company/k-j-consulting