The DIO Biotite-H Implant System is comprised of dental implant, surgical instruments and prosthetic components. The DIG BIOTITE -H Implant System is designed for conventional two-stage…
The DIO Biotite-H Implant System is comprised of dental implant, surgical instruments and prosthetic components. The DIG BIOTITE -H Implant System is designed for conventional two-stage procedures for single and multiple unit prosthetics. The DIO Biotite-H Implant System’s screw-form dental implant consist of machined titanium. Screw’s Diameter: Φ3.8mm, Φ4.1mm, Φ4.5mm, Φ4.8mm, Φ5.3mm. Length: 8.0mm, 10.mm, 12.0mm, 14.0mm. The implant’s raw material is titanium and its alloys for surgical implant applications (as perASTM-F-67, A-STM-F-136). The special implant surface is consists of 100% calcium phosphate(CaHPO 42H20). BioTite-H Implant System is an electrochemically deposited calcium phosphate coating based upon abiomimetic process in which implants are coated in an electrolytic bath with a 15+±- 5μm thin bioactive layer of a calcium phosphate composite. Biotite -H Implant System composed of the two calciumphosphates brushite(>95% )and HA(<5%).
Who Else Makes It
Concentrated in Jiangsu (3), Sichuan (2), Shanghai (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
Record
Regulatory record for DIO Biotite-H Implant System | Listed by | DIO Corporation, South Korea |
| FDA product code | DZE |
| Device type | Implant, Endosseous, Root-Form |
| Device class | Class 2 |
| Regulation | 21 CFR 872.3640 |
| Establishment | Repacker / relabeller, Manufacturer, Exporter |
| 510(k) | K073070 |
| Record published | 2015-10-17 |
| Record revised | 2022-02-25 (version 4) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date, manufacturing date, serial number |
| Storage | Special storage condition: tmperature limitation 1˚C ~ 30˚C, Humidity 80% |
| Distribution end date | 2022-02-04 |
| UDI direct marking | Exempt |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.