Home › Device types › OCJ
Spinal Channeling Instrument, Vertebroplasty
FDA product code OCJ · Class 1 · Orthopedic
96
Registered devices
20
Adverse events
2
Recalls
1
510(k) clearances
Devices with this code
BIOPSYBELL — BIOPSYBELL SRLBalloon Inflation Devices — Shanghai Lange Medtech Co., Ltd.CAPO Needle — NEXONE BIO CO., LTD.BIOPSYBELL — BIOPSYBELL SRLKyphoplasty Tool Kit — Jiangsu Changmei Medtech Co., Ltd.CAPO Needle — NEXONE BIO CO., LTD.BIOPSYBELL SRL — BIOPSYBELL SRLBIOPSYBELL — BIOPSYBELL SRLKiva — BENVENUE MEDICAL, INC.Mediox — Mediox Medical Service LtdBIOPSYBELL SRL — BIOPSYBELL SRLBIOPSYBELL — BIOPSYBELL SRLBIOPSYBELL — BIOPSYBELL SRLKeyFix Direct Access Needle — G21 SRLBANRAN-11 — RANFAC CORP.BIOPSYBELL SRL — BIOPSYBELL SRLBLAZER-C CURVED INJECTION SYSTEM-MV — Izi Medical Products, LLCBIOPSYBELL — BIOPSYBELL SRLBIOPSYBELL — BIOPSYBELL SRLBIOPSYBELL — BIOPSYBELL SRLNA — Synthes GmbHBIOPSYBELL — BIOPSYBELL SRLMain-AXS Needle-Spinal Simplicity — Mainstream Medical Devices, LLCBIOPSYBELL — BIOPSYBELL SRL
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-03-22 | DePuy Spine, Inc. | Mislabeled: Package labeled (11g x 6 inch) contains a 13g x 4-inch side hole needle |
| 2011-03-22 | DePuy Spine, Inc. | Mislabeled: Package labeled (11g x 6 inch) contains a 13g x 4-inch side hole needle |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.