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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 110 of 111
DeviceModel / ReferenceRegistriesClassStatus
CD73|NT5E, RM431, RMab BSB-3716-1
EUDAMEDFDA UDI
IVD GeneralActive
CD11c, EP157, RMab BSB 6448
EUDAMEDFDA UDI
IVD GeneralActive
Nanog, EP225, RMab BSB 3584
EUDAMEDFDA UDI
IVD GeneralActive
BG8 LewisY, F3, MMab BSB 6378
EUDAMEDFDA UDI
IVD GeneralActive
Tinto EGFR, 31G7, MMab BSB 5472
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Beta-Catenin, 14, MMab BSB 5086
EUDAMEDFDA UDI
IVD GeneralActive
p120 Catenin, EP66, RMab BSB 2082
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ALK-1|CD246, EP302, RMab BSB 2796
EUDAMEDFDA UDI
IVD GeneralActive
Cyclin B1, RM281, RMab BSB-3760-01
EUDAMEDFDA UDI
IVD GeneralActive
Glutamine Synthetase, GS-6, MMab BSB 2933
EUDAMEDFDA UDI
IVD GeneralActive
Alpha Synuclein, BSB-114, MMab BSB 3289
EUDAMEDFDA UDI
IVD GeneralActive
SOX-9, EP317, RMab BSB 3214
EUDAMEDFDA UDI
IVD GeneralActive
CD13, 38C12, MMab BSB 6327
EUDAMEDFDA UDI
IVD GeneralActive
CXCR4|CD184|Fusin, EP394, RMab BSB-3720-1
EUDAMEDFDA UDI
IVD GeneralActive
TORC3|CRTC3, BSB-175, MMab BSB-3805-05
EUDAMEDFDA UDI
IVD GeneralActive
IgA, BSB-39, MMab BSB 5663
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Histone H3 Phospho, EP233, RMab BSB 2525
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD31, 1A10, MMab BSB 5219
EUDAMEDFDA UDI
IVD GeneralActive
pan-TRK, RBT-TRK, RMab BSB-2376-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IL-1b, BSB-139, MMab BSB-3706-3
EUDAMEDFDA UDI
IVD GeneralActive
CD15, BSB-119, MMab BSB 5188
EUDAMEDFDA UDI
IVD GeneralActive
Tinto INI-1, 25, MMab BSB 6830
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD99, BSB-9, MMab BSB 5310
EUDAMEDFDA UDI
IVD GeneralActive
Epstein Barr Virus LMP-1, CS1-4, MMab BSB 5487
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GCDFP-15, 23A3, MMab BSB 5555
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Myeloperoxidase, Polyclonal, RPab BSB 5785
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 35BH11, 35BetaH11, MMab BSB 5422
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HHV-8, RBT-HHV8, RMab BSB-3778-7
EUDAMED
IVD GeneralActive
TNFa-IP2, BSB-141, MMab BSB-3708-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Desmoglein-3, EP306, RMab BSB 2894
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mesothelial Cell, HBME-1, MMab BSB 3455
EUDAMEDFDA UDI
IVD GeneralActive
SDHB, BSB-131, MMab BSB-2375-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Retinoblastoma| Rb, 1F8, MMab BSB 6129
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD68, BSB-8, MMab BSB 5289
EUDAMEDFDA UDI
IVD GeneralActive
CD38, SPC32, MMab BSB 6202
EUDAMEDFDA UDI
IVD GeneralActive
CD7, EP132, RMab BSB 2324
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TSH, BSB-56, MMab BSB 5995
EUDAMEDFDA UDI
IVD GeneralActive
Neurofilament, EP79, RMab BSB 2018
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 18, EP30, RMab BSB 6700
EUDAMEDFDA UDI
IVD GeneralActive
IgM, BSB-41, MMab BSB 5684
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GAB1|GRB2-associated-binding protein 1, BSB-155, MMab BSB-3727-3
EUDAMEDFDA UDI
IVD GeneralActive
Mart-1|Melan-A, M2-7C10, MMab BSB 5754
EUDAMEDFDA UDI
IVD GeneralActive
HER-3|c-erbB-3, RBT-HER3, RMab BSB 2632
EUDAMEDFDA UDI
IVD GeneralActive
Tinto S-100, 4C4.9, MMab BSB 5919
EUDAMEDFDA UDI
IVD GeneralActive
Surfactant protein D|SP-D, BSB-162, MMab BSB-3747-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto BAP1, BSB-109, MMab BSB 3301
EUDAMEDFDA UDI
IVD GeneralActive
Parathyroid Hormone|PTH, BSB-24, MMab BSB 2088
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 19, BSB-34, MMab BSB 2735
EUDAMEDFDA UDI
IVD GeneralActive
EpCAM|Epithelial Specific Antigen, Ber-EP4, MMab BSB 6279
EUDAMEDFDA UDI
IVD GeneralActive
hPL, Polyclonal, RPab BSB 6805
EUDAMEDFDA UDI
IVD GeneralActive

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