DIO IMPLANT SYSTEMS
- Primary DI
- 08800049233436
- Brand
- DIO IMPLANT SYSTEMS
- Company
- DIO Corporation
- Model
- ABN 40504
- Catalog number
- ABN 40504
- Device description
- The DIO Implant System includes one-stage fixture and two-stage fixture made of titanium. These implants are surgically inserted into the upper and/or lower jawbone, and serve as a substitute or replacement tooth root providing a stable foundation for restorations.
- Published
- 2022-03-01
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| NHA | Abutment, Implant, Dental, Endosseous |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| NHA | Abutment, Implant, Dental, Endosseous | Dental | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K070570 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 08800049233436 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 08800049233436 | 08800049233436 | 8800049233436 |
GMDN Terms#
| Term | Definition |
|---|---|
| Screw endosteal dental implant, two-piece | A sterile device made of alloplastic materials [e.g., titanium (Ti), stainless steel, ceramic] intended to be surgically implanted into alveolar and/or basal bone of the mandible or maxilla to provide support and a means of retention for a dental prosthesis (e.g., bridge, single-tooth, overdenture). It is a two-piece device composed of an anchorage component (implant body) in the form of a threaded screw that is implanted into bone, and a retention component (implant abutment), typically attached to the anchorage component after implantation, that protrudes through gingival tissues to support the prosthesis. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Storage Environment Temperature | 1 Degrees Celsius | 30 Degrees Celsius |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| 213-365-2875 | usahq@dioimplantusa.com |
Regulatory Flags#
- DUNS number
- 631085206
- Device count
- 1
- DM exempt
- true
- Lot or batch
- true
- Serial number
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 08800049245330 | Healing Cap | HCI 48504[H] | 2025-09-19 | |
| 08800049245361 | Healing Cap | HCI 65704[H] | 2025-09-19 | |
| 08800049245422 | Cemented Cylinder | ICC 48508[H] | 2025-09-19 | |
| 08800049245460 | Cemented Cylinder | ICC 48588[H] | 2025-09-19 | |
| 08800049245507 | Cemented Cylinder | ICC 60649[H] | 2025-09-19 | |
| 08800049245545 | Cemented Cylinder | ICC 65309[H] | 2025-09-19 | |
| 08800049416884 | Temporary Cylinder | ITC 48010 | 2025-09-19 | |
| 08806169097729 | Healing Cap | HCI 60704[H] | 2025-09-19 | |
| 08800049414217 | DIOnavi Guide | GUIDE 02 A01(a,b) | 2025-09-18 | |
| 08800049414231 | DIOnavi Guide | GUIDE 02 A02(a,b) | 2025-09-18 | |
| 08800049414255 | DIOnavi Guide | GUIDE 02 A03(a,b) | 2025-09-18 | |
| 08800049414279 | DIOnavi Guide | GUIDE 02 A04(a,b) | 2025-09-18 | |
| 08800049414293 | DIOnavi Guide | GUIDE 02 A05(a,b) | 2025-09-18 | |
| 08800049438961 | UF(II) Eastab Cylinder | ESMC 4812N | 2025-09-18 | |
| 08800049438985 | UF(II) Eastab Cylinder | ESMC 4812H | 2025-09-18 | |
| 08800049438992 | UF(II) Eastab Cylinder Semi Final | ESMCSF 4806N | 2025-09-18 | |
| 08800049443040 | UF(II) Eastab Cylinder Semi Final | ESMCSF 4806H | 2025-09-18 | |
| 08800049282892 | Pre-milled Bar | CBMC 02H | 2025-09-16 | |
| 08800049282908 | Pre-milled Bar | CBMC 02N | 2025-09-16 | |
| 08800049283448 | Pre-milled Bar | CBZN 01 | 2025-09-16 |
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