Biotem Co., ltd
South Korea Last updated 22 Oct 2026
- Devices
- 1,418
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
Biotem SAAT55644 Ref SAAT55644
Biotem HAB50604 Ref HAB50604
Biotem STFA5013 Ref STFA5013
Biotem STD20085 Ref STD20085
Biotem IAT4011MN Ref IAT4011MN
Biotem FDBH41L Ref FDBH41L
Biotem SAAT30524M Ref SAAT30524M
Biotem HAA553S Ref HAA553S
Biotem SAAS55655 Ref SAAS55655
Biotem FD21RL Ref FD21RL
Biotem SAAS55625 Ref SAAS55625
Biotem SABT40525 Ref SABT40525
Biotem FXIR4810W Ref FXIR4810W
Biotem BTTD46085 Ref BTTD46085
Biotem AABT40415 Ref AABT40415
Biotem FXBR5015R Ref FXBR5015R
Biotem FDIM31OL Ref FDIM31OL
Biotem AABT40225 Ref AABT40225
Biotem FXIR4811 Ref FXIR4811
Biotem AAAT50225B Ref AAAT50225B
Biotem FXIR4811M Ref FXIR4811M
Biotem SAAT65717 Ref SAAT65717
Biotem FXIR3510M Ref FXIR3510M
Biotem BTTD46130 Ref BTTD46130
Biotem SAAT65755 Ref SAAT65755
Biotem AAITB35415 Ref AAITB35415
Biotem SAAS45547 Ref SAAS45547
Biotem SAAT30517M Ref SAAT30517M
Biotem HAB50605 Ref HAB50605
Biotem CSA3300S Ref CSA3300S
Biotem BTTD51100 Ref BTTD51100
Biotem SABT50615 Ref SABT50615
Biotem AABT50415 Ref AABT50415
Biotem AAIT35415 Ref AAIT35415
Biotem FXIR3508M Ref FXIR3508M
Biotem FD25RS Ref FD25RS
Biotem LAIS4855 Ref LAIS4855
Biotem SAAT45535 Ref SAAT45535
Biotem SAAS55645 Ref SAAS55645
Biotem FXBR4013R Ref FXBR4013R
Biotem SAAS45545 Ref SAAS45545
Biotem FDIH31OL Ref FDIH31OL
Biotem FXIR4807W Ref FXIR4807W
Biotem STFA4010 Ref STFA4010
Biotem BTTD46075 Ref BTTD46075
Biotem IPI4808M Ref IPI4808M
Biotem HAA555S Ref HAA555S
Biotem SAAT65734 Ref SAAT65734
Biotem STFA5007 Ref STFA5007
Biotem STFA3515 Ref STFA3515
Showing 1,301-1,350 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