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Sign in to claim this brandWARANTEC.Co., Ltd
US
Last updated May 23, 2026
What WARANTEC.Co., Ltd makes
WARANTEC.Co., Ltd manufactures dental implant systems, including fixtures, abutments, and temporary cylinders. The company also produces reusable dental and maxillofacial surgical procedure kits, as well as various drill bits, drivers, adapters, and removal tools for dental applications.
The company is based in the US, and its portfolio consists of Class I and Class II medical devices. These products are listed in the FDA UDI database.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does WARANTEC.Co., Ltd manufacture?
WARANTEC.Co., Ltd specializes in dental implant systems, which include components such as fixtures, abutments, and temporary cylinders. Additionally, the company produces reusable dental and maxillofacial surgical procedure kits, along with various specialized tools including drill bits, drivers, adapters, and removal tools used in dental applications.
Where is WARANTEC.Co., Ltd based?
WARANTEC.Co., Ltd is based in the United States. This location information is provided as part of the company's official profile within the regulatory registry data.
How are the devices from WARANTEC.Co., Ltd classified?
The medical devices manufactured by WARANTEC.Co., Ltd are classified as Class I and Class II devices. These classifications are based on the regulatory framework under which the company's dental implant systems, surgical kits, and associated tools are categorized.
Where can I find a list of devices manufactured by WARANTEC.Co., Ltd?
The devices produced by WARANTEC.Co., Ltd are listed in the FDA UDI database. This registry serves as the official source for identifying the specific medical devices manufactured by the company.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 688857820
Catalogue (642)
Page 10 of 13| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| IU SB Abutment_Non hex Φ5.0 | IUSB5054N | FDA UDI | Class II | Active |
| IU SB Abutment Φ4.0 | IUSB4034A | FDA UDI | Class II | Active |
| IU SB Abutment_Non hex Φ4.0 | IUSB4054N | FDA UDI | Class II | Active |
| UT Fixture | FUT53100 | FDA UDI | Class II | Active |
| Bone Well | 5702 | FDA UDI | Class I | Active |
| Tap Drill | TD48130N | FDA UDI | Class I | Active |
| Bone Collecting Drill | SD-45-S | FDA UDI | Class I | Active |
| Twist Drill Stopper | S13 | FDA UDI | Class I | Active |
| IU SB Abutment Φ6.0 | IUSB6047 | FDA UDI | Class II | Active |
| IU SB Abutment Φ6.0 | IUSB6067 | FDA UDI | Class II | Active |
| Tap Drill | TD38085N | FDA UDI | Class I | Active |
| IU SB Abutment_Non hex Φ4.0 | IUSB4037NA | FDA UDI | Class II | Active |
| IU Healing Abutment | IUHA4050 | FDA UDI | Class II | Active |
| IU SB Abutment Φ5.0 | IUSB5034 | FDA UDI | Class II | Active |
| IU Twist Drill Short | SD-20-S | FDA UDI | Class I | Active |
| IU SB Abutment Φ5.0 | IUSB5017 | FDA UDI | Class II | Active |
| IU Fixture | FIU40100 | FDA UDI | Class II | Active |
| IU SB Abutment_hex Φ6.0 | IUSB6045H | FDA UDI | Class II | Active |
| IU Healing Abutment | IUHA4030A | FDA UDI | Class II | Active |
| IU Fixture | FIU40115 | FDA UDI | Class II | Active |
| Fixture Driver_handpiece type Short | HD-IU-RS | FDA UDI | Class I | Active |
| IT Twist Drill Long | D20-L | FDA UDI | Class I | Active |
| IU SB Abutment_Non hex Φ5.0 | IUSB5045N | FDA UDI | Class II | Active |
| IU Ball Attachment Abutment | IUBA4050A | FDA UDI | Class II | Active |
| IU SB Abutment Φ4.0 | IUSB4034 | FDA UDI | Class II | Active |
| Point Drill | PD | FDA UDI | Class I | Active |
| IU SB Abutment_Non hex Φ4.0 | IUSB4055N | FDA UDI | Class II | Active |
| Sinus Drill | SRM-28 | FDA UDI | Class I | Active |
| IU Implant Impression Post Pick-Up type Long | IUPPL | FDA UDI | Class I | Active |
| Final Drill | PD-30 | FDA UDI | Class I | Active |
| Bone Collecting Drill | SD-45-L | FDA UDI | Class I | Active |
| IU Fixture | FIU60085 | FDA UDI | Class II | Active |
| Bone Collecting Drill Stopper | DS-7 | FDA UDI | Class I | Active |
| IU SB Abutment_hex Φ5.0 | IUSB5067H | FDA UDI | Class II | Active |
| IU SB Abutment_Non hex Φ4.0 | IUSB4015N | FDA UDI | Class II | Active |
| IU Guide Screw Remover A Type_non hex | UG-SR-NA | FDA UDI | Class I | Active |
| IT Single-unit Analog | IC0SAN50H | FDA UDI | Class I | Active |
| IU SB Abutment Φ5.0 | IUSB5037 | FDA UDI | Class II | Active |
| IU SB Abutment Φ4.0 | IUSB4025A | FDA UDI | Class II | Active |
| IU SB Abutment_Non hex Φ5.0 | IUSB5067N | FDA UDI | Class II | Active |
| IU SB Abutment_Non hex Φ6.0 | IUSB6057N | FDA UDI | Class II | Active |
| IU SB Abutment_hex Φ4.0 | IUSB4035HA | FDA UDI | Class II | Active |
| Sinus Reamer | SRM-80 | FDA UDI | Class I | Active |
| Step Drill | SD36130 | FDA UDI | Class I | Active |
| IU Healing Abutment | IUHA4060 | FDA UDI | Class II | Active |
| IU SB Abutment_Non hex Φ4.0 | IUSB4045NA | FDA UDI | Class II | Active |
| UT Fixture | FUT43085 | FDA UDI | Class II | Active |
| Fixture Remover Screw | S2.5 | FDA UDI | Class I | Active |
| Sinus Curette | 7094 | FDA UDI | Class I | Active |
| IU Guide Screw Remover A Type_hex | UG-SR-HA | FDA UDI | Class I | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- WARANTEC Co., Ltd. Seongnam-si Gyeonggi · KR FEI 3009514134