Neobiotech Co., Ltd.
Neobiotech Co., Ltd. appears in FDA public data with 0 recalls, 17 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Apr 30, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 17
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K232528 | Protective Cap | Apr 30, 2024 |
| K232049 | IS-III active Short Implant | Mar 28, 2024 |
| K210903 | IS Multi Unit Abutment System | Jul 23, 2021 |
| K190849 | IS-III active System_S-narrow Type | Aug 14, 2019 |
| K181137 | IT-III active System | Nov 16, 2018 |
| K181138 | IS-III active System | Oct 3, 2018 |
| K181178 | S-mini active Fixture | Jul 24, 2018 |
| K173938 | IS-III HActive Fixture | May 24, 2018 |
| K160991 | Neo GBR System | Jan 10, 2017 |
| K120503 | CMI IMPLANT IS II ACTIVE | Jun 18, 2012 |
| K113554 | CMI IMPLANT IS SYSTEM | Apr 5, 2012 |
| K112540 | S-MINI IMPLANT SYSTEM | Feb 3, 2012 |
| K111761 | NEO TITANIUM MESH, CTI-MEM | Jan 10, 2012 |
| K090377 | SINUS QUICK EB SYSTEM | Aug 28, 2009 |
| K090825 | SQ IS SYSTEM | Jul 16, 2009 |
| K090527 | SINUS QUICK IT SYSTEM | Jul 14, 2009 |
| K042339 | NEOPLANT IMPLANT SYSTEM | Nov 2, 2004 |