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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 79 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto Herpes Simplex Virus I and II, 10A3 and BSB-116, MMab BSB 3469
EUDAMED
IVD GeneralActive
Tinto Cytokeratin 20, EP23, RMab BSB 6703
EUDAMEDFDA UDI
IVD GeneralActive
Tinto OCT-4, EP143, RMab BSB 2028
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 19, BSB-34, MMab BSB 2736
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CXCR4|CD184|Fusin, EP394, RMab BSB-3720-7
EUDAMEDFDA UDI
IVD GeneralActive
IgD|FITC, Polyclonal, GPab BSB-3006-1
EUDAMEDFDA UDI
IVD GeneralActive
Amyloid A, EP335, RMab BSB 2806
EUDAMEDFDA UDI
IVD GeneralActive
CDK2, RBT-CDK2, RMab BSB 2639
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PSMA, EP192, RMab BSB 6347
EUDAMEDFDA UDI
IVD GeneralActive
Alpha Synuclein, BSB-114, MMab BSB 3291
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Glucagon, EP74, RMab BSB 2328
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgG4, EP138, RMab BSB 6815
EUDAMEDFDA UDI
IVD GeneralActive
CD34, EP88, RMab BSB 6489
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MDR-1, JSB-1, MMab BSB 6898
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD14, EP128, RMab BSB 6458
EUDAMEDFDA UDI
IVD GeneralActive
CD7, LP15, MMab BSB 5167
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C1q, Polyclonal, RPab BSB 3021
EUDAMEDFDA UDI
IVD GeneralActive
GATA3, L50-823, MMab BSB 2675
EUDAMEDFDA UDI
IVD GeneralActive
Chromogranin A, LK2H10, MMab BSB 5349
EUDAMEDFDA UDI
IVD GeneralActive
Fascin, BSB-36, MMab BSB 5516
EUDAMEDFDA UDI
IVD GeneralActive
CD13, 38C12, MMab BSB 6329
EUDAMEDFDA UDI
IVD GeneralActive
NRAS, RBT-NRAS, RMab BSB 2668
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CA19-9, 121SLE, MMab BSB 5107
EUDAMEDFDA UDI
IVD GeneralActive
Inhibin Alpha, R1, MMab BSB 5692
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FOXP3, Polyclonal, RPab BSB 6759
EUDAMEDFDA UDI
IVD GeneralActive
Ksp-Cadherin, 4H6|F9, MMab BSB 6285
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD42b, EP409, RMab BSB 3506
EUDAMEDFDA UDI
IVD GeneralActive
SALL4, 6E3, MMab BSB 3186
EUDAMEDFDA UDI
IVD GeneralActive
Tinto AMACRacemase|P504S, 13H4, RMab BSB 5059
EUDAMEDFDA UDI
IVD GeneralActive
Treponema pallidum, Polyclonal, RPab BSB 3237
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Thymidylate synthase|TS, BSB-160, MMab BSB-3750-7
EUDAMEDFDA UDI
IVD GeneralActive
CD14, 7, MMab BSB 6314
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TTF-1, 8G7G3|1, MMab BSB 6001
EUDAMEDFDA UDI
IVD GeneralActive
Tinto bcl-10, BSB-22, MMab BSB 2700
EUDAMEDFDA UDI
IVD GeneralActive
Tinto INI-1, 25, MMab BSB 6828
EUDAMEDFDA UDI
IVD GeneralActive
c-Met|HGFR, EP1454Y, RMab BSB 6587
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ATM, EP327, RMab BSB-3710-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto STAT6, EP325, RMab BSB 3420
EUDAMEDFDA UDI
IVD GeneralActive
SALL4, 6E3, MMab BSB 3188
EUDAMEDFDA UDI
IVD GeneralActive
IMP-3|1GF2BP3, EP286, RMab BSB 2969
EUDAMEDFDA UDI
IVD GeneralActive
Glucagon, BSB-111, MMab BSB 3346
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 7, RM284, RMab BSB-3764-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cyclin E1, EP126, RMab BSB 6555
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Chromogranin A, LK2H10, MMab BSB 5346
EUDAMEDFDA UDI
IVD GeneralActive
Tinto hGAL|GCET2, EP316, RMab BSB 2936
EUDAMEDFDA UDI
IVD GeneralActive
EGFR Phospho, EP11, RMab BSB 6719
EUDAMEDFDA UDI
IVD GeneralActive
S-100, 4C4.9, MMab BSB 5922
EUDAMEDFDA UDI
IVD GeneralActive
Tinto bcl-2, BSB-5, MMab BSB 5072
EUDAMEDFDA UDI
IVD GeneralActive
Myosin Smooth Muscle, BSB-17, MMab BSB 5928
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgA|FITC, Polyclonal, GPab BSB-3005-3
EUDAMEDFDA UDI
IVD GeneralActive

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