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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 80 of 111
DeviceModel / ReferenceRegistriesClassStatus
pan-TRK, RM423, RMab BSB-3742-01
EUDAMED
IVD GeneralActive
Tinto c-Myc, EP121, RMab BSB 6578
EUDAMEDFDA UDI
IVD GeneralActive
IgM, BSB-41, MMab BSB 5683
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Fumarate Hydratase|Fumarase, BSB-151, MMab BSB-3726-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MCM2, RBT-MCM2, RMab BSB 6331
EUDAMEDFDA UDI
IVD GeneralActive
Claudin-7, EP399, RMab BSB-3719-05
EUDAMEDFDA UDI
IVD GeneralActive
IL-1b, BSB-139, MMab BSB-3706-1
EUDAMEDFDA UDI
IVD GeneralActive
Androgen Receptor, BSB-4, MMab BSB 6074
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Glucagon, BSB-111, MMab BSB 3342
EUDAMEDFDA UDI
IVD GeneralActive
IgD|FITC, Polyclonal, GPab BSB-3006-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PRAME, RBT-PRAME, RMab BSB-2374-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CITED1, BSB-177, MMab BSB-3808-15
EUDAMEDFDA UDI
IVD GeneralActive
DOG-1, RBT-DOG1, RMab BSB 6272
EUDAMEDFDA UDI
IVD GeneralActive
CD3, RBT-CD3, RMab BSB 6426
EUDAMEDFDA UDI
IVD GeneralActive
TLE1, 1F5, MMab BSB 2318
EUDAMEDFDA UDI
IVD GeneralActive
EGFR Phospho, EP11, RMab BSB 6721
EUDAMEDFDA UDI
IVD GeneralActive
IgG|FITC, Polyclonal, GPab BSB-3007-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SOX-11, CL0142, MMab BSB 2218
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Prostein|P501S, EP381, RMab BSB 3163
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Caspase-3, RM250, RMab BSB-3715-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HER-3|c-erbB-3, RBT-HER3, RMab BSB 2631
EUDAMEDFDA UDI
IVD GeneralActive
bcl-6, BSB-26, MMab BSB 3439
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Melanoma Cocktail: HMB-45, Mart-1 and Tyrosinase, HMB-45, A103 and BSB-6, MMab BSB-3695-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Estrogen Receptor, RBT-11, RMab BSB 5493
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Kappa Light Chains, BSB-58, MMab BSB 5702
EUDAMEDFDA UDI
IVD GeneralActive
Factor VIII-Related Antigen, Polyclonal, RPab BSB 5501
EUDAMEDFDA UDI
IVD GeneralActive
NUT|NUTM1, RBT-NUTM1, RMab BSB-3793-01
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast MiTF, C5 and D5, MMab BSB 3659
EUDAMEDFDA UDI
IVD GeneralActive
Prolactin, PRL02, MMab BSB 5894
EUDAMEDFDA UDI
IVD GeneralActive
Neurofilament, 2F11, MMab BSB 5817
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TMPRSS2, BSB-136, MMab BSB-3703-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Fibrinogen, Polyclonal, RPab BSB 3049
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SV40, Pab101, MMab BSB 2232
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 14, RM328, RMab BSB-3762-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto pan-TRK, RM423, RMab BSB-3742-7
EUDAMED
IVD GeneralActive
Tinto Melanoma KBA.62, KBA.62, MMab BSB 6906
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Osteonectin|SPARC, BSB-93, MMab BSB 3258
EUDAMEDFDA UDI
IVD GeneralActive
PMS2, EP51, RMab BSB 2123
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD56, 123C3.D5, MMab BSB 5267
EUDAMEDFDA UDI
IVD GeneralActive
IgM| FITC, Polyclonal, RPab BSB-3008-05
EUDAMEDFDA UDI
IVD GeneralActive
ROS-1, EP282, RMab BSB 3626
EUDAMEDFDA UDI
IVD GeneralActive
CD15, BSB-119, MMab BSB 5187
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LH, BSB-53, MMab BSB 5724
EUDAMEDFDA UDI
IVD GeneralActive
PELP1, RBT-PELP1, RMab BSB-3744-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 5 and 6, D5 and 16B4, MMab BSB 5400
EUDAMEDFDA UDI
IVD GeneralActive
Histone H3 Phospho, EP233, RMab BSB 2527
EUDAMEDFDA UDI
IVD GeneralActive
Tinto EpCAM|Epithelial Specific Antigen, Ber-EP4, MMab BSB 6276
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD11b, EP45, RMab BSB 6438
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD8, C8|144B, MMab BSB 5169
EUDAMEDFDA UDI
IVD GeneralActive
T-Bet|TBX-2, EP263, RMab BSB 2606
EUDAMEDFDA UDI
IVD GeneralActive

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