Biotem Co., ltd
South Korea Last updated 22 Oct 2026
- Devices
- 1,418
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
Biotem LAAF4015 Ref LAAF4015
Biotem AATT50225 Ref AATT50225
Biotem FXIR4808W Ref FXIR4808W
Biotem SAAT65735 Ref SAAT65735
Biotem HAB41507 Ref HAB41507
Biotem STFA4511 Ref STFA4511
Biotem HAI60702 Ref HAI60702
Biotem SAAT55624 Ref SAAT55624
Biotem BTTD42115 Ref BTTD42115
Biotem IAT6014SN Ref IAT6014SN
Biotem SAAT45565N Ref SAAT45565N
Biotem IAT4014SN Ref IAT4014SN
Biotem SAAT55665N Ref SAAT55665N
Biotem SAAT30525M Ref SAAT30525M
Biotem CSB5001 Ref CSB5001
Biotem TD46 Ref TD46
Bone Cup BPC07D20 Ref BPC07D20
Biotem SAAT45534 Ref SAAT45534
Biotem SAAS45515 Ref SAAS45515
Biotem FDBM4112C Ref FDBM4112C
Biotem SAAS65745 Ref SAAS65745
Biotem HAA555M Ref HAA555M
Biotem FXTR5007R Ref FXTR5007R
Biotem CDA4013S Ref CDA4013S
Biotem AAAT50425B Ref AAAT50425B
Biotem SAAS65735 Ref SAAS65735
Biotem FXBR4011R Ref FXBR4011R
Biotem FDBH41S Ref FDBH41S
Biotem BTTD51130 Ref BTTD51130
Biotem BTTD51075 Ref BTTD51075
Biotem FXIR4015M Ref FXIR4015M
Biotem SAAS65765 Ref SAAS65765
Biotem FXIR4008M Ref FXIR4008M
Biotem HAT50602 Ref HAT50602
Biotem SAAT45525 Ref SAAT45525
Biotem DS130 Ref DS130
Biotem BTTD51085 Ref BTTD51085
Biotem FDBH50S Ref FDBH50S
Biotem BTTD37075 Ref BTTD37075
Biotem FD25HL Ref FD25HL
Biotem LAIS48355 Ref LAIS48355
Biotem FXBR3713R Ref FXBR3713R
Biotem SAAT55635N Ref SAAT55635N
Biotem FXIR3515M Ref FXIR3515M
Biotem STFA4508 Ref STFA4508
Biotem STFA3511 Ref STFA3511
Biotem STD20075 Ref STD20075
Biotem CST5000 Ref CST5000
Bone Pen Drill BPAD02M Ref BPAD02M
Biotem SAAT55665 Ref SAAT55665
Showing 1,351-1,400 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