Biotem Co., ltd
South Korea Last updated 22 Oct 2026
- Devices
- 1,418
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
Biotem STFA3507 Ref STFA3507
Biotem BTTD34075 Ref BTTD34075
Biotem SAAS65744 Ref SAAS65744
Biotem LAAS4505 Ref LAAS4505
Biotem SAAT45517 Ref SAAT45517
Biotem FXIR4808 Ref FXIR4808
Biotem IPI4812 Ref IPI4812
Biotem SAITB4826C Ref SAITB4826C
Biotem SAAS45534 Ref SAAS45534
Biotem SAAT45547N Ref SAAT45547N
Biotem SAAT65717N Ref SAAT65717N
Biotem HAI60706 Ref HAI60706
Biotem STD20 Ref STD20
Biotem DS075 Ref DS075
Biotem TD37 Ref TD37
Biotem AAAT60225B Ref AAAT60225B
Biotem LAAF3715 Ref LAAF3715
Biotem IPA3413 Ref IPA3413
Biotem SAIS48434 Ref SAIS48434
Biotem IAT4014M Ref IAT4014M
Biotem SAAT45545 Ref SAAT45545
Biotem SABT50624 Ref SABT50624
Biotem HAT50604 Ref HAT50604
Biotem SAAS65714 Ref SAAS65714
Biotem FXBR6008RS Ref FXBR6008RS
Biotem HAA453S Ref HAA453S
Biotem SAAT30545M Ref SAAT30545M
Biotem HAA453M Ref HAA453M
Biotem FXTR5008R Ref FXTR5008R
Biotem SAAT55615N Ref SAAT55615N
Biotem SAAS30517M Ref SAAS30517M
Biotem SAAS55665 Ref SAAS55665
Biotem IPA3410 Ref IPA3410
Biotem SAAT55647N Ref SAAT55647N
Biotem FXTR5015R Ref FXTR5015R
Biotem BTTD34115 Ref BTTD34115
Biotem SAAT55634 Ref SAAT55634
Biotem HAA553M Ref HAA553M
Biotem HAA455M Ref HAA455M
Biotem SAAT30535M Ref SAAT30535M
Bone Cup BPC06D20 Ref BPC06D20
Biotem SAAT30527M Ref SAAT30527M
Biotem ITB4108T Ref ITB4108T
Biotem FXTR5013R Ref FXTR5013R
Biotem SD12RL Ref SD12RL
Biotem SABT50644 Ref SABT50644
Biotem HAI48601 Ref HAI48601
Biotem HAI48603 Ref HAI48603
Biotem HAA457S Ref HAA457S
Biotem SAAT45537 Ref SAAT45537
Showing 1,051-1,100 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