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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 90 of 111
DeviceModel / ReferenceRegistriesClassStatus
Progesterone Receptor, BSB-2, MMab BSB 2130
EUDAMEDFDA UDI
IVD GeneralActive
CA-125, OC125, MMab BSB 5095
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 4, EP4, RMab BSB 6590
EUDAMEDFDA UDI
IVD GeneralActive
Vimentin, EP21, RMab BSB 2312
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CDK2, RBT-CDK2, RMab BSB 2638
EUDAMEDFDA UDI
IVD GeneralActive
Androgen Receptor, BSB-4, MMab BSB 6075
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cyclin B1, RM281, RMab BSB-3760-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TLE1, RBT-TLE1, RMab BSB-3794-3
EUDAMEDFDA UDI
IVD GeneralActive
Glucagon, EP74, RMab BSB 2332
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Myoglobin, EP87, RMab BSB 6983
EUDAMEDFDA UDI
IVD GeneralActive
CD11b, EP45, RMab BSB 6439
EUDAMEDFDA UDI
IVD GeneralActive
TRAcP, 9C5, MMab BSB 5984
EUDAMEDFDA UDI
IVD GeneralActive
CD61, 2f2, MMab BSB 5286
EUDAMEDFDA UDI
IVD GeneralActive
INI-1, RBT-INI1, RMab BSB-3779-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD73|NT5E, RM431, RMab BSB-3716-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ZFAND3, BSB-169, MMab BSB-3797-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgD|FITC, Polyclonal, GPab BSB-3006-7
EUDAMEDFDA UDI
IVD GeneralActive
Desmin, D33, MMab BSB 5460
EUDAMEDFDA UDI
IVD GeneralActive
Tinto c-Met|HGFR, EP1454Y, RMab BSB 6585
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NeuN, A60, MMab BSB 2009
EUDAMEDFDA UDI
IVD GeneralActive
Tinto EMA, E29, MMab BSB 5477
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p16, RM267, RMab BSB-3768-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MNDA, BSB-157, MMab BSB-3738-7
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast p63, 4A4, MMab BSB-3698-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MDM2, BSB-64, MMab BSB 2980
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Fascin, BSB-36, MMab BSB 5512
EUDAMEDFDA UDI
IVD GeneralActive
Prostein|P501S, EP381, RMab BSB 3165
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Napsin A, EP205, RMab BSB 6989
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Candida Albicans, RBT-C.alb, RMab BSB-3803-15
EUDAMED
IVD GeneralActive
Tinto p16, RM267, RMab BSB-3768-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD38, SPC32, MMab BSB 6198
EUDAMEDFDA UDI
IVD GeneralActive
CD105|Endoglin, EP274, RMab BSB 2870
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Caveolin-1, EP353, RMab BSB 3314
EUDAMEDFDA UDI
IVD GeneralActive
Tinto E-Cadherin, EP6, RMab BSB 5464
EUDAMEDFDA UDI
IVD GeneralActive
TCR Delta, BSB-127, MMab BSB 3649
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUM1, EP190, RMab BSB 6953
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast EpCAM, Ber-EP4, MMab BSB 3680
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MMP-9, EP127, RMab BSB 2539
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LMO2, RBT-LM02, RMab BSB 3574
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SV40, Pab101, MMab BSB 2230
EUDAMEDFDA UDI
IVD GeneralActive
CD105|Endoglin, EP274, RMab BSB 2871
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast MART-1, A103, MMab BSB 3651
EUDAMEDFDA UDI
IVD GeneralActive
Tinto INSM1, BSB-123, MMab BSB 3554
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD117, EP10, RMab BSB 5318
EUDAMEDFDA UDI
IVD GeneralActive
B7H3|CD276, RBT-B7H3, RMab BSB 2815
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MSH2, RBT-MSH2, RMab BSB 6928
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast p40, ZR8, RMab BSB-3697-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC2, BSB-45, MMab BSB 6158
EUDAMEDFDA UDI
IVD GeneralActive
Tinto hPL, EP241, RMab BSB 2414
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD31, 1A10, MMab BSB 5220
EUDAMEDFDA UDI
IVD GeneralActive

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