K&J Consulting Corp.
Lansdale, PA, US
K&J Consulting Corp. appears in FDA device records in Lansdale, PA. FDA records list 6 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for K&J Consulting Corp. between 2021 and 2025. The busiest year on record is 2023, with 4. The most recent is 2025, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2021 | 1 |
| 2023 | 4 |
| 2025 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K250335 | IVA & AEON Cervical and Lumbar Cage System | ODP | Substantially Equivalent | |
| K232877 | FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System | MRW | Substantially Equivalent | |
| K233332 | Statera-C™ Spinal System | NKG | Substantially Equivalent | |
| K232586 | Rexious Spinal Fixation System, Statera™ Spinal System, Statera-M™ Spinal System | NKB | Substantially Equivalent | |
| 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 | KWQ | Substantially Equivalent | |
| K212038 | K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage | ODP | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain