Home › Device types › NPK
Barrier, Synthetic, Intraoral
FDA product code NPK · Class 2 · Dental
248
Registered devices
83
Adverse events
1
Recalls
31
510(k) clearances
Devices with this code
Cytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical IncRPM™ Reinforced PTFE Mesh — Osteogenics Biomedical IncCytoflex Ti-enforced — UNICARE BIOMEDICAL INC.Cytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical IncRPM™ Reinforced PTFE Mesh — Osteogenics Biomedical IncSalvin Dental Specialties — SALVIN DENTAL SPECIALTIES, LLCOpenTex — PURGO BIOLOGICS Inc.RPM™ Reinforced PTFE Mesh — Osteogenics Biomedical IncRPM™ Reinforced PTFE Mesh — Osteogenics Biomedical IncOpenTex — PURGO BIOLOGICS Inc.Cytoflex Textured Tef-Guard — UNICARE BIOMEDICAL INC.Neoss Implant System — Neoss ABcreos™ syntoprotect — Nobel Biocare ABRPM™ Reinforced PTFE Mesh — Osteogenics Biomedical IncRPM™ Reinforced PTFE Mesh — Osteogenics Biomedical IncCytoflex Ti-enforced — UNICARE BIOMEDICAL INC.GUIDOR — SUNSTAR AMERICAS, INC.Cytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical IncMEDPOR CONTAIN — Stryker Leibinger GmbH & Co. KGOpenTex — PURGO BIOLOGICS Inc.creos™ syntoprotect — Nobel Biocare ABRPM™ Reinforced PTFE Mesh — Osteogenics Biomedical IncCytoplast™ Titanium-Reinforced PTFE Membranes — Osteogenics Biomedical IncInion GTR™ — Inion Oy
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-03-01 | Inion Ltd. | Aluminum pouch seal was noticed to be defective (slightly open). |
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.