Home › Device types › NPK
Barrier, Synthetic, Intraoral
FDA product code NPK · Class 2 · Dental
252
Registered devices
83
Adverse events
1
Recalls
31
510(k) clearances
Devices with this code
InnoGenic™ Non-resorbable Membrane-InnoGenic™ Wifi-Mesh — Cowellmedi Co.,LtdCytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical IncCytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical IncInnoGenic™ Non-resorbable Membrane-InnoGenic™ PTFE-Mesh — Cowellmedi Co.,LtdCytoflex Ti-enforced — UNICARE BIOMEDICAL INC.MEDPOR CONTAIN — Stryker Leibinger GmbH & Co. KGCytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical IncCytoflex Ti-enforced — UNICARE BIOMEDICAL INC.Neoss Implant System — Neoss ABCytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical IncOpenTex — PURGO BIOLOGICS Inc.OpenTex — PURGO BIOLOGICS Inc.Cytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical IncCytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical Inccreos™ syntoprotect — Nobel Biocare ABCytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical Inccreos™ syntoprotect — Nobel Biocare ABRPM™ Reinforced PTFE Mesh — Osteogenics Biomedical IncCytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical IncMEDPOR CONTAIN — Stryker Leibinger GmbH & Co. KGcreos™ syntoprotect — Nobel Biocare ABNeoss Implant System — Neoss ABRPM™ Reinforced PTFE Mesh — Osteogenics Biomedical IncRPM™ Reinforced PTFE Mesh — Osteogenics Biomedical Inc
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-03-01 | Inion Ltd. | Aluminum pouch seal was noticed to be defective (slightly open). |
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