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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 111 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto Osteonectin|SPARC, BSB-93, MMab BSB 3260
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GLUT1, EP141, RMab BSB 6780
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SALL4, 6E3, MMab BSB 3184
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NeuN, A60, MMab BSB 2008
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ALK-1|CD246, EP302, RMab BSB 2797
EUDAMEDFDA UDI
IVD GeneralActive
Inhibin alpha, EP378, RMab BSB 3361
EUDAMEDFDA UDI
IVD GeneralActive
Trop-2|EGP-1, BSB-148, MMab BSB-3754-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p40, ZR8, RMab BSB 2072
EUDAMEDFDA UDI
IVD GeneralActive
CD33, RBT-CD33, RMab BSB 3452
EUDAMEDFDA UDI
IVD GeneralActive
PAX-7, BSB-145, MMab BSB-3743-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Parafibromin, BSB-50, MMab BSB 2747
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Claudin-5, EP224, RMab BSB 2399
EUDAMEDFDA UDI
IVD GeneralActive
Mart-1|Melan-A, A103, MMab BSB 6874
EUDAMEDFDA UDI
IVD GeneralActive
Annexin A1, BSB-95, MMab BSB 6363
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC1, RBT-MUC1, RMab BSB-3788-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Uroplakin III, Polyclonal, RPab BSB 2287
EUDAMEDFDA UDI
IVD GeneralActive
iNOS, RBT-iNOS, RMab BSB 2659
EUDAMEDFDA UDI
IVD GeneralActive
C3c|FITC, Polyclonal, RPab BSB-3002-05
EUDAMEDFDA UDI
IVD GeneralActive
MUC1, BSB-44, MMab BSB 6154
EUDAMEDFDA UDI
IVD GeneralActive
Mammaglobin, EP249, RMab BSB 5746
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Napsin A, RBT-NAPSA, RMab BSB-3789-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p21, DCS-60.2, MMab BSB 2063
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HER-2 neu, RBT-HER2, RMab BSB 2036
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Caspase-3, RM250, RMab BSB-3715-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Thymidylate synthase|TS, BSB-160, MMab BSB-3750-3
EUDAMEDFDA UDI
IVD GeneralActive
TRAcP, 9C5, MMab BSB 5983
EUDAMEDFDA UDI
IVD GeneralActive
Glypican-3, 1G12, MMab BSB 6243
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NeuN, RBT-NeuN, RMab BSB-3781-3
EUDAMEDFDA UDI
IVD GeneralActive
TRPS1, EP392, RMab BSB-3790-05
EUDAMEDFDA UDI
IVD GeneralActive
CD8, C8|144B, MMab BSB 5173
EUDAMEDFDA UDI
IVD GeneralActive
Insulin, BSB-42, MMab BSB 5697
EUDAMEDFDA UDI
IVD GeneralActive
MUC-4, EP256, RMab BSB 2555
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Glycophorin A, GA-R2 (HIR2), MMab BSB 5583
EUDAMEDFDA UDI
IVD GeneralActive
CD43, MT1, MMab BSB 5242
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Villin, EP163, RMab BSB 2301
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mycobacterium tuberculosis, Polyclonal, RPab BSB 2993
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 19, EP72, RMab BSB 5384
EUDAMEDFDA UDI
IVD GeneralActive
GFAP, RM246, RMab BSB-3766-1
EUDAMEDFDA UDI
IVD GeneralActive
MDR-1, JSB-1, MMab BSB 6901
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin HMW 34BE12, 34BetaE12, MMab BSB 5394
EUDAMEDFDA UDI
IVD GeneralActive
MSH6, 44, MMab BSB 6147
EUDAMEDFDA UDI
IVD GeneralActive
bcl-2, BSB-5, MMab BSB 5075
EUDAMEDFDA UDI
IVD GeneralActive
Thyroglobulin, BSB-49, MMab BSB 5976
EUDAMEDFDA UDI
IVD GeneralActive
GFAP, G-A-5, MMab BSB 5564
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NRAS, RBT-NRAS, RMab BSB 2665
EUDAMEDFDA UDI
IVD GeneralActive
CD20, L26, MMab BSB 5194
EUDAMEDFDA UDI
IVD GeneralActive
Amyloid A, EP335, RMab BSB 2807
EUDAMEDFDA UDI
IVD GeneralActive

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