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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 72 of 111
DeviceModel / ReferenceRegistriesClassStatus
HIF-1alpha, EP118, RMab BSB 2522
EUDAMEDFDA UDI
IVD GeneralActive
TDP-43|TARDBP, BSB-166, MMab BSB-3776-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto BAP1, BSB-109, MMab BSB 3300
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Ki-67, RM360, RMab BSB-3767-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Annexin VII, EP367, RMab BSB-3709-7
EUDAMEDFDA UDI
IVD GeneralActive
BRAF V600E, RM8, RMab BSB 2827
EUDAMED
IVD GeneralActive
Cytokeratin 35BH11, 35BetaH11, MMab BSB 5426
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CDK2, RBT-CDK2, RMab BSB 2637
EUDAMEDFDA UDI
IVD GeneralActive
MSH2, RBT-MSH2, RMab BSB 6929
EUDAMEDFDA UDI
IVD GeneralActive
bcl-6, EP278, RMab BSB 2822
EUDAMEDFDA UDI
IVD GeneralActive
INSM1, RBT-INSM1, RMab BSB-3780-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto OLIG2, EP112, RMab BSB 2559
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C4d, EP272, RMab BSB 2831
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD13, 38C12, MMab BSB 6324
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 19, RM364, RMab BSB-3763-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin OSCAR, OSCAR, MMab BSB 6179
EUDAMEDFDA UDI
IVD GeneralActive
Tinto bcl-6, BSB-26, MMab BSB 3436
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD3, RBT-CD3, RMab BSB 6423
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NeuN, RBT-NeuN, RMab BSB-3781-7
EUDAMEDFDA UDI
IVD GeneralActive
Caldesmon, BSB-19, MMab BSB 6104
EUDAMEDFDA UDI
IVD GeneralActive
ALK-1|CD246, EP302, RMab BSB 2799
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 17, BSB-33, MMab BSB 2731
EUDAMEDFDA UDI
IVD GeneralActive
Tinto INI-1, RBT-INI1, RMab BSB-3779-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p27, SX53G8, MMab BSB 5835
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Caspase-3, RM250, RMab BSB-3715-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GATA3, L50-823, MMab BSB 2671
EUDAMEDFDA UDI
IVD GeneralActive
FOXP1, EP137, RMab BSB 6755
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Prostein|P501S, EP381, RMab BSB 3164
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Glucagon, EP74, RMab BSB 2330
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin MNF116, MNF116, MMab BSB 3533
EUDAMEDFDA UDI
IVD GeneralActive
TTF-1, 8G7G3|1, MMab BSB 6004
EUDAMEDFDA UDI
IVD GeneralActive
Topoisomerase IIa, RBT-Topo2a, RMab BSB 6343
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD23, EP75, RMab BSB 6473
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Villin, CWWB1, MMab BSB 6016
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HMGA2, EP398, RMab BSB-3729-15
EUDAMEDFDA UDI
IVD GeneralActive
Uroplakin III, Polyclonal, RPab BSB 2290
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CTLA-4|CD152, RBT-CTLA-4, RMab BSB 3484
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 14, LL002, MMab BSB 6223
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Annexin A1, BSB-95, MMab BSB 6359
EUDAMEDFDA UDI
IVD GeneralActive
p16, 16P04, JC2, MMab BSB 5830
EUDAMEDFDA UDI
IVD GeneralActive
IMP-3|1GF2BP3, EP286, RMab BSB 2967
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Myeloperoxidase, EP151, RMab BSB 6967
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD44, BSB-12, MMab BSB 6235
EUDAMEDFDA UDI
IVD GeneralActive
Tinto pan-TRK, RBT-TRK, RMab BSB-2376-3
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin MNF116, MNF116, MMab BSB 3537
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC2, EP187, RMab BSB 6947
EUDAMEDFDA UDI
IVD GeneralActive
Maspin, BSB-92, MMab BSB 3270
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MDM2, BSB-64, MMab BSB 2979
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IDH1 R132H, RBT-IDH1, RMab BSB-3732-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SMAD4|DPC4, BSB-63, MMab BSB 3205
EUDAMEDFDA UDI
IVD GeneralActive

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