Biotem Co., ltd
South Korea Last updated 22 Oct 2026
- Devices
- 1,418
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
Biotem SAAT65735N Ref SAAT65735N
Biotem SAAS45527 Ref SAAS45527
Biotem HAA552S Ref HAA552S
Biotem SAAT55645N Ref SAAT55645N
Biotem BTTD34100 Ref BTTD34100
Biotem SAIT40434 Ref SAIT40434
Biotem IAT5014SN Ref IAT5014SN
Biotem CDA6013S Ref CDA6013S
Biotem FXBR3308R Ref FXBR3308R
Biotem HAA652S Ref HAA652S
Biotem SAAT65725 Ref SAAT65725
Biotem SAAS30637M Ref SAAS30637M
Biotem SAAS45555 Ref SAAS45555
Biotem IAT4014MN Ref IAT4014MN
Biotem SAAT65714 Ref SAAT65714
Biotem SAAT65724 Ref SAAT65724
Biotem TD2329 Ref TD2329
Biotem FXIR5511 Ref FXIR5511
Biotem LAIS48357 Ref LAIS48357
Biotem FXBR3708R Ref FXBR3708R
Biotem ITB3511T Ref ITB3511T
Biotem STFA5011 Ref STFA5011
Biotem CDA4513S Ref CDA4513S
Biotem STFA4515 Ref STFA4515
Biotem AAAT45215Q Ref AAAT45215Q
Biotem SAAT65724N Ref SAAT65724N
Biotem SAAS45524 Ref SAAS45524
Biotem HAB35402 Ref HAB35402
Biotem AAAT60425B Ref AAAT60425B
Biotem SAAT45527 Ref SAAT45527
Biotem HDB0908 Ref HDB0908
Biotem SAAS55615 Ref SAAS55615
Biotem AABT35415 Ref AABT35415
Biotem BTTD42085 Ref BTTD42085
Biotem SABT50614 Ref SABT50614
Biotem SAAS65717 Ref SAAS65717
Biotem SAAT55644N Ref SAAT55644N
Biotem FXIR5513 Ref FXIR5513
Biotem DS115 Ref DS115
Biotem AAAT55225Q Ref AAAT55225Q
Biotem CDA4011T Ref CDA4011T
Biotem FDBM5008 Ref FDBM5008
Biotem SABT40524 Ref SABT40524
Biotem HAA455S Ref HAA455S
Biotem STFA3510 Ref STFA3510
Biotem SABT50645 Ref SABT50645
Biotem FXIR4808M Ref FXIR4808M
Biotem FXIR5510 Ref FXIR5510
Biotem AAIT35425 Ref AAIT35425
Biotem FXBR5007R Ref FXBR5007R
Showing 1,201-1,250 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