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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 92 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto IgG4, BSB-96, MMab BSB 6807
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 35BH11, 35BetaH11, MMab BSB 5421
EUDAMEDFDA UDI
IVD GeneralActive
p21, DCS-60.2, MMab BSB 2067
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgE, Polyclonal, RPab BSB 3068
EUDAMEDFDA UDI
IVD GeneralActive
PD-L1|CD274, RBT-PDL1, RMab BSB 2654
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Inhibin Alpha, R1, MMab BSB 5687
EUDAMEDFDA UDI
IVD GeneralActive
Helicobacter Pylori, BSB-37, MMab BSB 2682
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Parvovirus, R92F6, MMab BSB 5855
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PLA2R1, BSB-129, MMab BSB-2372-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Amyloid Beta, RBT-A4, RMab BSB 3443
EUDAMEDFDA UDI
IVD GeneralActive
Tinto EMA, E29, MMab BSB 5479
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TCL1, EP105, RMab BSB 2253
EUDAMEDFDA UDI
IVD GeneralActive
Tinto BCA-225, Cu-18, MMab BSB 5066
EUDAMEDFDA UDI
IVD GeneralActive
C4d, EP272, RMab BSB 2835
EUDAMEDFDA UDI
IVD GeneralActive
p16, 16P04, JC2, MMab BSB 5832
EUDAMEDFDA UDI
IVD GeneralActive
Progesterone Receptor, EP2, RMab BSB 2577
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p16, 16P04, JC2, MMab BSB 5829
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Lysozyme, EP134, RMab BSB 6857
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SMAD4|DPC4, BSB-63, MMab BSB 3206
EUDAMEDFDA UDI
IVD GeneralActive
Tinto bcl-6, RBT-bcl6, RMab BSB 5079
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C1q|FITC, Polyclonal, RPab BSB-3001-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Helicobacter pylori, Polyclonal, RPab BSB 5605
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CXCR4|CD184|Fusin, EP394, RMab BSB-3720-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto A-1-Antichymotrypsin, EP384, RMab BSB 3499
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Vimentin, V9, MMab BSB 6022
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Helicobacter Pylori, BSB-37, MMab BSB 2678
EUDAMEDFDA UDI
IVD GeneralActive
MUC5AC, CLH2, MMab BSB 6168
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Lambda|FITC, Polyclonal, GPab BSB-3010-7
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 20, Ks20.8, MMab BSB 5391
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Napsin A, BSB-112, MMab BSB 3392
EUDAMEDFDA UDI
IVD GeneralActive
OLIG2, EP112, RMab BSB 2563
EUDAMEDFDA UDI
IVD GeneralActive
PLAP, BSB-47, MMab BSB 2757
EUDAMEDFDA UDI
IVD GeneralActive
Glypican-3, 1G12, MMab BSB 6245
EUDAMEDFDA UDI
IVD GeneralActive
CA19-9, 121SLE, MMab BSB 5110
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Albumin|FITC, polyclonal, RPab BSB-3000-3
EUDAMEDFDA UDI
IVD GeneralActive
SMAD4|DPC4, BSB-63, MMab BSB 3208
EUDAMEDFDA UDI
IVD GeneralActive
SV40, Pab101, MMab BSB 2235
EUDAMEDFDA UDI
IVD GeneralActive
p21, DCS-60.2, MMab BSB 2068
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SALL4, 6E3, MMab BSB 3183
EUDAMEDFDA UDI
IVD GeneralActive
ARID1A, EP303, RMab BSB-3749-01
EUDAMEDFDA UDI
IVD GeneralActive
PTEN, RM265, RMab BSB-3769-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PTEN, RBT-PTEN, RMab BSB 2645
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD10, 56C6, MMab BSB 5177
EUDAMEDFDA UDI
IVD GeneralActive
SOX-10, BSB-62, MMab BSB 2212
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Musashi 2, RM422, RMab BSB-3740-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Islet 1|ISL1, EP283, RMab BSB 2972
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Zap-70, 2F3.2, MMab BSB 6036
EUDAMEDFDA UDI
IVD GeneralActive
OLIG2, EP112, RMab BSB 2562
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Gastrin, Polyclonal, RPab BSB 5547
EUDAMEDFDA UDI
IVD GeneralActive
Gastrin, Polyclonal, RPab BSB 5550
EUDAMEDFDA UDI
IVD GeneralActive

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