Identity
- Trade Name
- Ti-one 101 FDA UDI
- Generic Name
- Dental implant system FDA UDI
- Device Name
- Abutment Ø4.5, 4 mm Abt. H The Ti-one 101 Dental Implant System is a device made of pure titanium metal and titanium alloy intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, and to restore the patient's chewing function. It consists of fixture, abutment, mount, mount screw, cover screw, impression coping, analog, impression coping screw and plastic impression cap. Its materials, dimensions, and intended use are similar to devices currently marketed worldwide. FDA UDI
- Model / Reference
- HF01-203040 FDA UDI
- Description
- Abutment Ø4.5, 4 mm Abt. H The Ti-one 101 Dental Implant System is a device made of pure titanium metal and titanium alloy intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, and to restore the patient's chewing function. It consists of fixture, abutment, mount, mount screw, cover screw, impression coping, analog, impression coping screw and plastic impression cap. Its materials, dimensions, and intended use are similar to devices currently marketed worldwide. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04719871590300 FDA UDI
- 510(k) Number
- K110425 FDA UDI
- FDA Product Code
- NHA FDA UDI
- GMDN Term
- Dental implant system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3630 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Safe FDA UDI
Category: Dental implant system
Ti-one 101 by Hung Chun Bio-S Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental implant system.
- Healing abutment Regular — BIO CONCEPT Co., Ltd. · Class II
- Ball Attachment 5 mm — NOGA MEDICAL PRODUCTS LTD · Class II
- Equator Abutment, Φ 6.5mm, GH 2mm — BIO CONCEPT Co., Ltd. · Class II
- Short Abutment — InnoBioSurg Co., Ltd(IBS implant Co., Ltd) · Class II
- Magicore — InnoBioSurg Co., Ltd(IBS implant Co., Ltd) · Class II
- Magicore S — InnoBioSurg Co., Ltd(IBS implant Co., Ltd) · Class II
- Implant Regular — BIO CONCEPT Co., Ltd. · Class II
- TRI — Tri Dental Implants Int. AG · Class II
Cleared under the same submission
K110425 also covers:
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
- Ti-one 101 — Hung Chun Bio-S Co., Ltd.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Hung Chun Bio-S Co., Ltd.
Sources (1)
- FDA UDI b7fcaf33-0337-4b9c-951a-5c651a110255 34 fields · synced Jun 8, 2026