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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 96 of 111
DeviceModel / ReferenceRegistriesClassStatus
hPL, EP241, RMab BSB 2417
EUDAMEDFDA UDI
IVD GeneralActive
NeuN, RBT-NeuN, RMab BSB-3781-01
EUDAMEDFDA UDI
IVD GeneralActive
TIGIT, BSB-152, MMab BSB-3751-01
EUDAMEDFDA UDI
IVD GeneralActive
PAX-8, RM436, RMab BSB-3786-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Ki-67, EP5, RMab BSB 5710
EUDAMEDFDA UDI
IVD GeneralActive
PAX-2, EP235, RMab BSB 2570
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TIGIT, BSB-152, MMab BSB-3751-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C3c|FITC, Polyclonal, RPab BSB-3002-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MiTF, C5 and D5, MMab BSB 6248
EUDAMEDFDA UDI
IVD GeneralActive
Parafibromin, BSB-50, MMab BSB 2751
EUDAMEDFDA UDI
IVD GeneralActive
Tinto COX-2, RBT-COX2, RMab BSB 5358
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD57, BSB-10, MMab BSB 5276
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD14, 7, MMab BSB 6311
EUDAMEDFDA UDI
IVD GeneralActive
Somatostatin Receptor 2|SSTR2, EP149, RMab BSB-3748-01
EUDAMEDFDA UDI
IVD GeneralActive
Mart-1|Melan-A, M2-7C10, MMab BSB 5755
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mart-1|Melan-A, M2-7C10, MMab BSB 5750
EUDAMEDFDA UDI
IVD GeneralActive
ALK-1|CD246, RBT-ALK1, RMab BSB 5046
EUDAMEDFDA UDI
IVD GeneralActive
Aspergillus, RBT-A.fumi, RMab BSB-3804-1
EUDAMED
IVD GeneralActive
Carbonic Anhydrase 9, EP161, RMab BSB 6418
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Myeloperoxidase, EP151, RMab BSB 6968
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Beta-Catenin, 14, MMab BSB 5087
EUDAMEDFDA UDI
IVD GeneralActive
CD23, 1B12, MMab BSB 5207
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD45RA, 4KB5, MMab BSB 5253
EUDAMEDFDA UDI
IVD GeneralActive
B7H3|CD276, RBT-B7H3, RMab BSB 2814
EUDAMEDFDA UDI
IVD GeneralActive
Glycophorin A, GA-R2 (HIR2), MMab BSB 5585
EUDAMEDFDA UDI
IVD GeneralActive
TRPS1, EP392, RMab BSB-3790-1
EUDAMEDFDA UDI
IVD GeneralActive
Herpes Simplex Virus I and II, 10A3 and BSB-116, MMab BSB 3473
EUDAMED
IVD GeneralActive
Tinto CD71, 10F11, MMab BSB 6520
EUDAMEDFDA UDI
IVD GeneralActive
Somatostatin Receptor 2|SSTR2, EP149, RMab BSB-3748-1
EUDAMEDFDA UDI
IVD GeneralActive
MLH1, G168-728, MMab BSB 5768
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ERCC1, EP219, RMab BSB 2483
EUDAMEDFDA UDI
IVD GeneralActive
LMO2, RBT-LM02, RMab BSB 3577
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mammaglobin, EP249, RMab BSB 5744
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Renal Cell Carcinoma, PN-15, MMab BSB 5912
EUDAMEDFDA UDI
IVD GeneralActive
Villin, CWWB1, MMab BSB 6020
EUDAMEDFDA UDI
IVD GeneralActive
IgG|FITC, Polyclonal, GPab BSB-3007-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Prolactin, PRL02, MMab BSB 5890
EUDAMEDFDA UDI
IVD GeneralActive
Albumin, polyclonal, RPab BSB 3017
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FOXL2, Polyclonal, RPab BSB-3725-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Macrophage HAM-56, HAM-56, MMab BSB 5736
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD15, BSB-119, MMab BSB 5184
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Glucagon, BSB-111, MMab BSB 3344
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC5AC, CLH2, MMab BSB 6164
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD6, BSB-54, MMab BSB 2707
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Tri-Methyl-Histone H3(Lys27)|H3K27Me3, RBT-H3K27Me3, RMab BSB-3806-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Trop-2|EGP-1, BSB-148, MMab BSB-3754-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CDX2, EP25, RMab BSB 6058
EUDAMEDFDA UDI
IVD GeneralActive
FSH, EP257, RMab BSB 3542
EUDAMEDFDA UDI
IVD GeneralActive
CD71, 10F11, MMab BSB 6523
EUDAMEDFDA UDI
IVD GeneralActive
HMGA2, EP398, RMab BSB-3729-1
EUDAMEDFDA UDI
IVD GeneralActive

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