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BIO SB, INC.

United States·US-MF-000036462

Last updated September 17, 2026

What BIO SB, INC. makes

Bio SB, Inc. manufactures in vitro diagnostic (IVD) products for immunohistochemistry, including chromogenic substrates, enzyme-linked detection kits, and antibody-based reagents. Their portfolio includes enzyme immunohistochemistry substrates like DAB and AEC, as well as specific detection antibodies such as cytokeratin and CD cell markers. Control slides and reagents for analytes like Helicobacter pylori, Candida albicans, and BAP1 are also produced, alongside specialized digestion solutions for tissue processing.

The company’s products are classified under FDA’s Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for laboratory use in diagnostic testing and are regulated under U.S. FDA guidelines. The manufacturer operates within the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Bio SB, Inc. manufacture?

Bio SB, Inc. specializes in in vitro diagnostic (IVD) products primarily used in immunohistochemistry (IHC) testing. Their portfolio includes chromogenic substrates like DAB (brown) and AEC (red) for enzyme-linked detection, antibody-based reagents for detecting specific analytes (such as cytokeratin and CD cell markers), and control slides for validation purposes. Examples include reagents for Helicobacter pylori, Candida albicans, and specialized tissue digestion solutions like the Mohs ImmunoDigestor. These products are designed for laboratory use in diagnostic workflows.

Where is Bio SB, Inc. based, and how does that affect its regulatory standing?

Bio SB, Inc. is based in the United States. Since it manufactures devices regulated by the FDA, its products must comply with U.S. regulatory requirements. The company’s devices fall under FDA’s Class I classification, which generally involves lower-risk devices requiring less stringent premarket review. However, compliance with FDA guidelines—such as listing in the UDI database—remains essential for market authorization.

Which regulatory registries or databases list Bio SB, Inc.’s devices?

Bio SB, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is a standardized way for the FDA to track and identify medical devices in the U.S. market. Listing in this database ensures traceability and compliance with FDA requirements for Class I devices, though it does not imply individual device approval—only that the manufacturer has registered their products as required.

How are Bio SB, Inc.’s devices classified by regulatory authorities?

Bio SB, Inc.’s devices are classified under the FDA’s Class I category. This classification is based on risk assessment: Class I devices are generally considered low-risk and pose minimal potential harm to users. As a result, they typically require less regulatory oversight than higher-risk classes (e.g., Class II or III), though they must still meet FDA compliance standards, such as proper labeling, manufacturing controls, and UDI registration. Classification does not guarantee market authorization—only that the device falls under a specific regulatory pathway.

What is the primary purpose of Bio SB, Inc.’s in vitro diagnostic (IVD) products?

Bio SB, Inc.’s IVD products are designed for laboratory use in immunohistochemistry (IHC) and related diagnostic testing. These include chromogenic substrates (e.g., DAB for brown staining), antibody reagents for detecting specific proteins (like cytokeratin or CD markers), and control slides to validate test accuracy. For example, their Helicobacter pylori control slides or BAP1 antibodies help pathologists confirm the presence of specific biomarkers in tissue samples. The products support accurate diagnostic workflows in clinical or research settings.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States
Address
5385 , Hollister Avenue, Santa Barbara, CA, United States
Website
biosb.com
LinkedIn
—
Facebook
—
Phone
+1(800)561-1145
PRRC Contact
Jessica Dunston
EUDAMED SRN
US-MF-000036462
FDA FEI Number
3008773547
DUNS Number
102855447

Catalogue (5547)

Page 85 of 111
DeviceModel / ReferenceRegistriesClassStatus
Napsin A, EP205, RMab BSB 6991
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 14, LL002, MMab BSB 6219
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Zap-70, 2F3.2, MMab BSB 6037
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 4, EP4, RMab BSB 6595
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LIN28, EP150, RMab BSB 3561
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Myosin Smooth Muscle, BSB-17, MMab BSB 5924
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Osteonectin|SPARC, BSB-93, MMab BSB 3259
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD73|NT5E, RM431, RMab BSB-3716-7
EUDAMEDFDA UDI
IVD GeneralActive
MCM2, RBT-MCM2, RMab BSB 6336
EUDAMEDFDA UDI
IVD GeneralActive
Tinto hPL, EP241, RMab BSB 2413
EUDAMEDFDA UDI
IVD GeneralActive
C3d, Polyclonal, RPab BSB 6391
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD79a, JCB117, MMab BSB 5302
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TdT, RBT-TdT, RMab BSB 2267
EUDAMEDFDA UDI
IVD GeneralActive
C1q, Polyclonal, RPab BSB 3022
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TdT, EP266, RMab BSB 2608
EUDAMEDFDA UDI
IVD GeneralActive
CD73|NT5E, RM431, RMab BSB-3716-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 14, LL002, MMab BSB 6221
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Claudin-5, EP224, RMab BSB 2398
EUDAMEDFDA UDI
IVD GeneralActive
Tinto S100A1, EP184, RMab BSB 2163
EUDAMEDFDA UDI
IVD GeneralActive
ICOS|CD278, RM417, RMab BSB-3731-01
EUDAMEDFDA UDI
IVD GeneralActive
Lamin-B1, RBT-LMNB1, RMab BSB-3735-1
EUDAMEDFDA UDI
IVD GeneralActive
CD10, 56C6, MMab BSB 5180
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Tyrosinase, BSB-6, MMab BSB 6009
EUDAMEDFDA UDI
IVD GeneralActive
Tinto BCA-225, Cu-18, MMab BSB 5065
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p16, 16P04, JC2, MMab BSB 5827
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Podoplanin, D2-40, MMab BSB-3699-7
EUDAMEDFDA UDI
IVD GeneralActive
TAG-72, BSB-21, MMab BSB 5956
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Surfactant protein D|SP-D, BSB-162, MMab BSB-3747-15
EUDAMEDFDA UDI
IVD GeneralActive
TIM-3|HAVCR2|CD366, BSB-163, MMab BSB-3752-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MAGEC2, EP405, RMab BSB-3795-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto S100A1, EP184, RMab BSB 2161
EUDAMEDFDA UDI
IVD GeneralActive
IgD, EP173, RMab BSB 2961
EUDAMEDFDA UDI
IVD GeneralActive
CD20, L26, MMab BSB 5193
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SOX-2, RM427, RMab BSB-3770-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Chromogranin A, LK2H10, MMab BSB 5345
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Aurora B, RM278, RMab BSB-3712-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD68, KP-1, MMab BSB 2712
EUDAMEDFDA UDI
IVD GeneralActive
CD45, 2B11 and PD7|26, MMab BSB 5249
EUDAMEDFDA UDI
IVD GeneralActive
Parathyroid Hormone|PTH, BSB-24, MMab BSB 2087
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Galectin-3, 9C4, MMab BSB 5541
EUDAMEDFDA UDI
IVD GeneralActive
Mammaglobin, EP249, RMab BSB 5748
EUDAMEDFDA UDI
IVD GeneralActive
IL-1b, BSB-139, MMab BSB-3706-05
EUDAMEDFDA UDI
IVD GeneralActive
ERCC1, EP219, RMab BSB 2485
EUDAMEDFDA UDI
IVD GeneralActive
Myeloperoxidase, EP151, RMab BSB 6970
EUDAMEDFDA UDI
IVD GeneralActive
Maspin, BSB-92, MMab BSB 3269
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD63, NKI|C3, MMab BSB 6296
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgA|FITC, Polyclonal, GPab BSB-3005-15
EUDAMEDFDA UDI
IVD GeneralActive
CD25, 4C9, MMab BSB 6320
EUDAMEDFDA UDI
IVD GeneralActive
CD11c, EP157, RMab BSB 6447
EUDAMEDFDA UDI
IVD GeneralActive
LIN28, EP150, RMab BSB 3563
EUDAMEDFDA UDI
IVD GeneralActive

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