Biotem Co., ltd
South Korea Last updated 22 Oct 2026
- Devices
- 1,418
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
Biotem LAIS604EW Ref LAIS604EW
Bone Pin BPP09D20 Ref BPP09D20
Biotem FXBR5013R Ref FXBR5013R
Biotem SAAS30537M Ref SAAS30537M
Biotem SAAS55624 Ref SAAS55624
Biotem FXIR4013 Ref FXIR4013
Biotem DS085 Ref DS085
Biotem AABT35215 Ref AABT35215
Bone Pen Drill BPAD02S Ref BPAD02S
Biotem BHS Ref BHS
Biotem IPB35412 Ref IPB35412
Biotem SABT40545 Ref SABT40545
Biotem SAAT45534N Ref SAAT45534N
Biotem LAIF4815 Ref LAIF4815
Biotem FXBR6015RS Ref FXBR6015RS
Biotem SATA4010 Ref SATA4010
Biotem HAT50605 Ref HAT50605
Biotem FD21HS Ref FD21HS
Biotem SAAT30544M Ref SAAT30544M
Biotem SAAS30627M Ref SAAS30627M
Biotem SAAT65747 Ref SAAT65747
Biotem SAAS65755 Ref SAAS65755
Biotem SAAS45565 Ref SAAS45565
Biotem AATT50425 Ref AATT50425
Biotem SAAT55645 Ref SAAT55645
Biotem FDIM29OS Ref FDIM29OS
Biotem SAAT45524 Ref SAAT45524
Biotem SAAT65737 Ref SAAT65737
Biotem IPB40512 Ref IPB40512
Biotem FXBR6013RS Ref FXBR6013RS
Biotem HAI48604 Ref HAI48604
Biotem LAAF3415 Ref LAAF3415
Biotem SAAS45535 Ref SAAS45535
Biotem HAI60704 Ref HAI60704
Biotem ITB5111T Ref ITB5111T
Biotem IAT5011SN Ref IAT5011SN
Biotem SABT35445 Ref SABT35445
Biotem SAAS30617M Ref SAAS30617M
Biotem SAAS65727 Ref SAAS65727
Biotem LAAS5507 Ref LAAS5507
Biotem STFA4510 Ref STFA4510
Biotem SAIS48357 Ref SAIS48357
Biotem SAAT55614 Ref SAAT55614
Biotem LAB5018 Ref LAB5018
Biotem LAIS4857 Ref LAIS4857
Biotem STD20130 Ref STD20130
Biotem HAB41503 Ref HAB41503
Biotem CSB4101 Ref CSB4101
Biotem FXBR3315R Ref FXBR3315R
Biotem FXIR4813M Ref FXIR4813M
Showing 951-1,000 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