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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 108 of 111
DeviceModel / ReferenceRegistriesClassStatus
hCG, BSB-38, MMab BSB 5601
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Spectrin, RBC2|3D5, MMab BSB 5939
EUDAMEDFDA UDI
IVD GeneralActive
FOXL2, Polyclonal, RPab BSB-3725-1
EUDAMEDFDA UDI
IVD GeneralActive
PU.1, EP18, RMab BSB 2157
EUDAMEDFDA UDI
IVD GeneralActive
Parafibromin, BSB-50, MMab BSB 2750
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FOXP3, Polyclonal, RPab BSB 6758
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CEACAM7, BSB-168, MMab BSB-3791-3
EUDAMEDFDA UDI
IVD GeneralActive
Lamin-B1, RBT-LMNB1, RMab BSB-3735-05
EUDAMEDFDA UDI
IVD GeneralActive
C3d, Polyclonal, RPab BSB 6390
EUDAMEDFDA UDI
IVD GeneralActive
DOG-1, EP332, RMab BSB 2906
EUDAMEDFDA UDI
IVD GeneralActive
Epstein Barr Virus LMP-1, CS1-4, MMab BSB 5489
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ATRX, RBT-ATRX, RMab BSB-3711-7
EUDAMEDFDA UDI
IVD GeneralActive
MUC2, BSB-45, MMab BSB 6161
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD138, B-A38, MMab BSB 5330
EUDAMEDFDA UDI
IVD GeneralActive
CD1a, EP80, RMab BSB 5137
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast p40, ZR8, RMab BSB-3697-3
EUDAMEDFDA UDI
IVD GeneralActive
bcl-2, BSB-5, MMab BSB 5074
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ATM, EP327, RMab BSB-3710-3
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Ki-67, RM360, RMab BSB-3771-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Actin Muscle Specific, HHF35, MMab BSB 5023
EUDAMEDFDA UDI
IVD GeneralActive
MUC6, CLH5, MMab BSB 6174
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HEG1, SKM9-2, MMab BSB-3728-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GH, EP267, RMab BSB 2498
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast p63, 4A4, MMab BSB-3698-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Beta-Catenin, 14, MMab BSB 5085
EUDAMEDFDA UDI
IVD GeneralActive
Estrogen Receptor, EP1, RMab BSB 2492
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Androgen Receptor, BSB-4, MMab BSB 6072
EUDAMEDFDA UDI
IVD GeneralActive
Caspase-3, RM250, RMab BSB-3715-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HHV-8, 13B10, MMab BSB 5645
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MGMT|AGAT, EP337, RMab BSB-3737-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin HMW 34BE12, 34BetaE12, MMab BSB 5393
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD45RO, UCHL-1, MMab BSB 5260
EUDAMEDFDA UDI
IVD GeneralActive
ARID1A, EP303, RMab BSB-3749-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto bcl-2, EP36, RMab BSB 6542
EUDAMEDFDA UDI
IVD GeneralActive
Hepatocyte Specific Antigen\Hep-Par1, OCH1E5, MMab BSB 5627
EUDAMEDFDA UDI
IVD GeneralActive
CD73|NT5E, RM431, RMab BSB-3716-05
EUDAMEDFDA UDI
IVD GeneralActive
Uroplakin III, EP321, RMab BSB 3243
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Helicobacter pylori, Polyclonal, RPab BSB 5603
EUDAMEDFDA UDI
IVD GeneralActive
TCR Beta, BSB-117, MMab BSB 2263
EUDAMEDFDA UDI
IVD GeneralActive
CD74, LN2, MMab BSB 5299
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SDHB, BSB-131, MMab BSB-2375-3
EUDAMEDFDA UDI
IVD GeneralActive
LAG-3|CD223, EP294, RMab BSB 3368
EUDAMEDFDA UDI
IVD GeneralActive
Gastrin, Polyclonal, RPab BSB 5552
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD123 IL-3Ra, BSB-59, MMab BSB 5325
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Neurofilament, EP79, RMab BSB 2016
EUDAMEDFDA UDI
IVD GeneralActive
CD10, 56C6, MMab BSB 5181
EUDAMEDFDA UDI
IVD GeneralActive
CD11b, EP45, RMab BSB 6441
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IL-1b, BSB-139, MMab BSB-3706-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Fibrinogen|FITC, Polyclonal, RPab BSB-3004-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SDHB, BSB-131, MMab BSB-2375-7
EUDAMEDFDA UDI
IVD GeneralActive

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