Biotem Co., ltd
South Korea Last updated 22 Oct 2026
- Devices
- 1,418
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
Biotem HAA457M Ref HAA457M
Biotem SD12RS Ref SD12RS
Biotem IPI4808 Ref IPI4808
Biotem SAAT45545N Ref SAAT45545N
Biotem FXBR3313R Ref FXBR3313R
Biotem FDIH29OS Ref FDIH29OS
Biotem FXBR5008R Ref FXBR5008R
Biotem FXBR6007RS Ref FXBR6007RS
Biotem BTTD34085 Ref BTTD34085
Biotem SAIT40437 Ref SAIT40437
Biotem LAAS6505 Ref LAAS6505
Biotem LAB4018 Ref LAB4018
Biotem IPI4812M Ref IPI4812M
Biotem SAAT55635 Ref SAAT55635
Biotem STFA4513 Ref STFA4513
Biotem BTTD60115 Ref BTTD60115
Biotem SAAS55617 Ref SAAS55617
Biotem FXIR4011M Ref FXIR4011M
Biotem IAT5014S Ref IAT5014S
Biotem SAAT55655 Ref SAAT55655
Biotem AAAT45425Q Ref AAAT45425Q
Biotem AAAT60215B Ref AAAT60215B
Biotem FXBR4015R Ref FXBR4015R
Biotem SAAT65744 Ref SAAT65744
Biotem HAA557S Ref HAA557S
Biotem SAAT55615 Ref SAAT55615
Biotem AABT35425 Ref AABT35425
Biotem BTTD60100 Ref BTTD60100
Biotem FD25RL Ref FD25RL
Biotem LAAS5505 Ref LAAS5505
Biotem SABT50634 Ref SABT50634
Biotem BTTD37130 Ref BTTD37130
Biotem DE Ref DE
Biotem FXIR4811W Ref FXIR4811W
Biotem FXIR4810M Ref FXIR4810M
Biotem SAIS48437 Ref SAIS48437
Biotem HAA657S Ref HAA657S
Biotem TD34 Ref TD34
Biotem SAAS55635 Ref SAAS55635
Biotem FXIR5515 Ref FXIR5515
Biotem FP21H Ref FP21H
Biotem SAIS48355 Ref SAIS48355
Biotem BTTD42100 Ref BTTD42100
Biotem SABT40527 Ref SABT40527
Biotem SAAS55627 Ref SAAS55627
Biotem HAA459S Ref HAA459S
Biotem IAT6011S Ref IAT6011S
Biotem FDBH35S Ref FDBH35S
Biotem SABT40514 Ref SABT40514
Biotem SAAT45515N Ref SAAT45515N
Showing 1,251-1,300 of 1,418
FDA establishments
- Biotem Co., Ltd. Busan · KR FEI 3009611645
What Biotem Co., ltd makes
Biotem Co., Ltd manufactures dental implant systems, including components designed for osseointegration in oral and maxillofacial applications. Their portfolio also includes bone pins, which are used for internal fixation in surgical procedures. The devices are intended for use in dental and orthopedic settings, supporting structural stability and integration with bone tissue.
The company’s products are regulated under the FDA’s classification system, with devices falling into Class I and Class II categories. These are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device regulations. The manufacturer operates from the United States.
Information
- Address
- 422, Sasang-ro, Busan, South Korea
- Website
- naver.com
- [email protected]
- PRRC contact
- Chang Kyu Hwang
- EUDAMED SRN
- KR-MF-000040891
- DUNS number
- 557793214