Biotem Co., ltd
South Korea Last updated 22 Oct 2026
- Devices
- 1,418
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
SAAS40534 Ref SAAS40534
PXFI4808WS Ref PXFI4808WS
SAAS30555M Ref SAAS30555M
FXIR4815MS Ref FXIR4815MS
PXFI4812S Ref PXFI4812S
ASTFA3511S Ref ASTFA3511S
FXTR6015RS Ref FXTR6015RS
Biotem SAAS30547M Ref SAAS30547M
Biotem AAITB6025W Ref AAITB6025W
Biotem FXIR4810 Ref FXIR4810
Biotem SAAT45514 Ref SAAT45514
Biotem FXIR4007M Ref FXIR4007M
Biotem SAAT55627N Ref SAAT55627N
Bone Pin BPP06D20 Ref BPP06D20
Biotem SAAT55614N Ref SAAT55614N
Biotem STFA4011 Ref STFA4011
Biotem FXIR4807M Ref FXIR4807M
Biotem FXBR4007R Ref FXBR4007R
Biotem SABT40547 Ref SABT40547
Biotem SAAS45517 Ref SAAS45517
Biotem DS100 Ref DS100
Biotem FDBM4108C Ref FDBM4108C
Biotem AABT50215 Ref AABT50215
Biotem SAAT65765 Ref SAAT65765
Biotem STFA3513 Ref STFA3513
Biotem SABT50625 Ref SABT50625
Biotem SAAT45555N Ref SAAT45555N
Biotem FDBH35L Ref FDBH35L
Biotem LAAS4507 Ref LAAS4507
Biotem CDA5011T Ref CDA5011T
Biotem FXBR3710R Ref FXBR3710R
Biotem IPA5810 Ref IPA5810
Biotem SAAT55617 Ref SAAT55617
Biotem SAAS55614 Ref SAAS55614
Biotem SAAT45514N Ref SAAT45514N
Biotem HAB41505 Ref HAB41505
Biotem FDBM3512C Ref FDBM3512C
Biotem FXIR4815 Ref FXIR4815
Biotem GD18 Ref GD18
Biotem FXIR4815M Ref FXIR4815M
Biotem HAI48602 Ref HAI48602
Biotem BTTD46100 Ref BTTD46100
Bone Pin BPP08D20 Ref BPP08D20
Biotem LAAS5504 Ref LAAS5504
Biotem HAB50602 Ref HAB50602
Biotem SAITB604EW Ref SAITB604EW
Biotem SAAS30647M Ref SAAS30647M
Biotem PP1820 Ref PP1820
Biotem SABT40517 Ref SABT40517
Biotem SAAS45544 Ref SAAS45544
Showing 851-900 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