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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 101 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto OX-40|CD134, BSB-90, MMab BSB 3122
EUDAMEDFDA UDI
IVD GeneralActive
CD21, EP64, RMab BSB 5200
EUDAMEDFDA UDI
IVD GeneralActive
MMP-9, EP127, RMab BSB 2541
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Amyloid Beta, RBT-A4, RMab BSB 3442
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Pneumocystis jirovecii, 3F6, MMab BSB 5877
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast SOX-10, BSB-62, MMab BSB 3654
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin Cocktail AE1 and AE3, AE1 and AE3, MMab BSB 5428
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Ksp-Cadherin, 4H6|F9, MMab BSB 6284
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PU.1, EP18, RMab BSB 2154
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SOX-9, EP317, RMab BSB 3213
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Tyrosinase, BSB-6, MMab BSB 6010
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PLAP, BSB-47, MMab BSB 2755
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Lamin-B1, RBT-LMNB1, RMab BSB-3735-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PTEN, RM265, RMab BSB-3769-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NKX3.1, RM430, RMab BSB-3785-15
EUDAMEDFDA UDI
IVD GeneralActive
C4d, EP272, RMab BSB 2834
EUDAMEDFDA UDI
IVD GeneralActive
GFAP, G-A-5, MMab BSB 5565
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD43, MT1, MMab BSB 5240
EUDAMEDFDA UDI
IVD GeneralActive
Tinto bcl-2, BSB-5, MMab BSB 5073
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ALK-1|CD246, RBT-ALK1, RMab BSB 5044
EUDAMEDFDA UDI
IVD GeneralActive
CD63, NKI|C3, MMab BSB 6299
EUDAMEDFDA UDI
IVD GeneralActive
Amyloid A, EP335, RMab BSB 2808
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PAX-2, EP235, RMab BSB 2568
EUDAMEDFDA UDI
IVD GeneralActive
TORC3|CRTC3, BSB-175, MMab BSB-3805-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto INSM1, RBT-INSM1, RMab BSB-3780-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HER-3|c-erbB-3, RBT-HER3, RMab BSB 2629
EUDAMEDFDA UDI
IVD GeneralActive
MUC1, BSB-44, MMab BSB 6153
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Adipophilin|ADRP, BSB-91, MMab BSB 3248
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD63, NKI|C3, MMab BSB 6297
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD43, MT1, MMab BSB 5241
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CXCR5|CD185, Polyclonal, RPab BSB-3721-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SOX-10, EP268, RMab BSB 2580
EUDAMEDFDA UDI
IVD GeneralActive
ERCC1, EP219, RMab BSB 2487
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Claudin-1, Polyclonal, RPab BSB 6562
EUDAMEDFDA UDI
IVD GeneralActive
Vimentin, V9, MMab BSB 6027
EUDAMEDFDA UDI
IVD GeneralActive
CXCL12|SDF-1, BSB-165, MMab BSB-3713-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LMO2, RBT-LM02, RMab BSB 3576
EUDAMEDFDA UDI
IVD GeneralActive
INI-1, RBT-INI1, RMab BSB-3779-1
EUDAMEDFDA UDI
IVD GeneralActive
GATA3, EP368, RMab BSB 3332
EUDAMEDFDA UDI
IVD GeneralActive
Calponin, BSB-20, MMab BSB 5124
EUDAMEDFDA UDI
IVD GeneralActive
Cyclin D3, BSB-171, MMab BSB-3799-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cathepsin K, BSB-172, MMab BSB-3800-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto BAP1, BSB-109, MMab BSB 3302
EUDAMEDFDA UDI
IVD GeneralActive
PD-1|CD279, NAT-105, MMab BSB 6217
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PAX-8, RM436, RMab BSB-3786-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Somatostatin Receptor 2|SSTR2, EP149, RMab BSB-3748-7
EUDAMEDFDA UDI
IVD GeneralActive
Napsin A, RBT-NAPSA, RMab BSB-3789-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Collagen Type IV, CIV22, MMab BSB 5353
EUDAMEDFDA UDI
IVD GeneralActive
PRAME, RBT-PRAME, RMab BSB-2374-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto WT1, 6F-H2, MMab BSB 6030
EUDAMEDFDA UDI
IVD GeneralActive

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