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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 105 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto CA15-3, DF3, MMab BSB 5100
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Histone H3 Phospho, EP233, RMab BSB 2524
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC2, BSB-45, MMab BSB 6156
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Podoplanin|D2-40, D2-40, MMab BSB 6064
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Alpha-Fetoprotein, BSB-23, MMab BSB 5052
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD3, RBT-CD3, RMab BSB 6424
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GH, EP267, RMab BSB 2496
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IDH1 R132H, IHC132, MMab BSB 3546
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Helicobacter Pylori, EP279, RMab BSB 3280
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TRPS1, EP392, RMab BSB-3790-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC4, 8G7, MMab BSB 2987
EUDAMEDFDA UDI
IVD GeneralActive
Tinto S100A1, EP184, RMab BSB 2162
EUDAMEDFDA UDI
IVD GeneralActive
Prealbumin|Transthyretin, BSB-125, MMab BSB 3621
EUDAMEDFDA UDI
IVD GeneralActive
Tinto OCT-4, EP143, RMab BSB 2030
EUDAMEDFDA UDI
IVD GeneralActive
Factor H|Complement Factor H, BSB-164, MMab BSB-3723-05
EUDAMEDFDA UDI
IVD GeneralActive
CXCR4|CD184|Fusin, EP394, RMab BSB-3720-05
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Chromogranin A, LK2H10, MMab BSB-3773-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Estrogen Receptor, RBT-11, RMab BSB 5491
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FGFR-3, BSB-150, MMab BSB-3724-3
EUDAMEDFDA UDI
IVD GeneralActive
C3c, Polyclonal, RPab BSB 3029
EUDAMEDFDA UDI
IVD GeneralActive
Epstein Barr Virus LMP-1, CS1-4, MMab BSB 5488
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Maspin, BSB-92, MMab BSB 3267
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Villin, CWWB1, MMab BSB 6017
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Pygopus 2|Pygo 2, BSB-156, MMab BSB-3745-7
EUDAMEDFDA UDI
IVD GeneralActive
CD31, 1A10, MMab BSB 5221
EUDAMEDFDA UDI
IVD GeneralActive
CD8, EP334, RMab BSB 2850
EUDAMEDFDA UDI
IVD GeneralActive
SMAD4|DPC4, RBT-SMAD4, RMab BSB 3404
EUDAMEDFDA UDI
IVD GeneralActive
IgG, BSB-40, MMab BSB 5677
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ACE2, BSB-135, MMab BSB-3702-7
EUDAMEDFDA UDI
IVD GeneralActive
AMACRacemase|P504S, 13H4, RMab BSB 5060
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Treponema pallidum, Polyclonal, RPab BSB 3234
EUDAMEDFDA UDI
IVD GeneralActive
Calretinin, RM324, RMab BSB-3757-01
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 19, EP72, RMab BSB 5382
EUDAMEDFDA UDI
IVD GeneralActive
Tinto S100P, EP186, RMab BSB 2184
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD1a, EP80, RMab BSB 5134
EUDAMEDFDA UDI
IVD GeneralActive
PLAP, EP194, RMab BSB 5873
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PU.1, EP18, RMab BSB 2155
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NGFR, BSB-18, MMab BSB 6290
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mart-1|Melan-A, M2-7C10, MMab BSB 5751
EUDAMEDFDA UDI
IVD GeneralActive
TSH, BSB-56, MMab BSB 5999
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD38, SPC32, MMab BSB 6200
EUDAMEDFDA UDI
IVD GeneralActive
CXCR4|CD184|Fusin, EP394, RMab BSB-3720-01
EUDAMEDFDA UDI
IVD GeneralActive
PTEN, RBT-PTEN, RMab BSB 2647
EUDAMEDFDA UDI
IVD GeneralActive
E-Cadherin, EP6, RMab BSB 5467
EUDAMEDFDA UDI
IVD GeneralActive
HER-3|c-erbB-3, RBT-HER3, RMab BSB 2634
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MSH2, BSB-147, MMab BSB-3722-3
EUDAMEDFDA UDI
IVD GeneralActive
Ki-67, EP5, RMab BSB 5711
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Fli-1, G146-222, MMab BSB 5521
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PDX1, EP139, RMab BSB 3155
EUDAMEDFDA UDI
IVD GeneralActive
SATB2, EP281, RMab BSB 3202
EUDAMEDFDA UDI
IVD GeneralActive

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