Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 46 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto OX-40/CD134 (BSB-90) BSB 3120 (ASR)
FDA UDI
Class IActive
Prolactin Control Slides Control Slides, 5
FDA UDI
Class IActive
Albumin Control Slides BSB-9008-CS
FDA UDI
Class IActive
Tinto c-Myc MMab Predilute, 7 ml
FDA UDI
Class IActive
Nuclear Fast Red Counterstainer 1000 ml
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector AEC HRP Red Detection System 15 ml each
FDA UDI
Class IActive
9-core PTEN Cell Line Microarray Control Slides Control Slides, 5
FDA UDI
Class IActive
Tinto Somatostatin RPab Predilute, 15 ml
FDA UDI
Class IActive
Tinto MSH6 (RBT-MSH6) BSB-3843-7
FDA UDI
Class IActive
Tinto Alpha-Fetoprotein RMab Predilute, 3 ml
FDA UDI
Class IActive
CD41/ Integrin alpha IIb control slides Control Slides, 5
FDA UDI
Class IActive
Tinto AldH1A1, RMab Predilute, 15 ml
FDA UDI
Class IActive
Uroplakin III Control Slides BSB-9424-CS
FDA UDI
Class IActive
BRG-1/SMARCA4 Control Slides BSB-9038-CS
FDA UDI
Class IActive
ImmnoDNA Background Blocker 50 ml
FDA UDI
Class IActive
IgE / FITC GPab Concentrate, 1 ml
FDA UDI
Class IActive
TdT RPab Concentrate, 0.5 ml
FDA UDI
Class IActive
5-core Melanoma Cell Line Microarray Control Slides Control Slides, 5
FDA UDI
Class IActive
PolyDetector Peroxidase Blocker 1000 ml
FDA UDI
Class IActive
Tinto T. cruzi (BSB-183) BSB-3838-15-ASR
FDA UDI
Class IActive
TintoPolyDetector Plus Red Detection Kit (300 Test) BSB-7462R
FDA UDI
Class IActive
CD19 RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
GH control slides Control Slides, 5
FDA UDI
Class IActive
CEA Control Slides Control Slides, 5
FDA UDI
Class IActive
Tinto Cytokeratin HMW AE3, MMab Predilute, 7 ml
FDA UDI
Class IActive
A-1-Antichymotrypsin control slides Control Slide, 5
FDA UDI
Class IActive
PolyDetector HRP Blue Plus BSB-0363-200
FDA UDI
Class IActive
Actin Smooth Muscle control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Thrombomodulin, RMab Predilute, 15 ml
FDA UDI
Class IActive
Tinto PAX-6 RMab Predilute, 7 ml
FDA UDI
Class IActive
CD103/ITGAE Control Slides BSB-9059-CS
FDA UDI
Class IActive
PiT1 Control Slides BSB-9453-CS
FDA UDI
Class IActive
p40 control slides Control Slides, 5
FDA UDI
Class IActive
c-Met/HGFR Control Slides BSB-9039-CS
FDA UDI
Class IActive
XyGreen PermaMounter 500 ml
FDA UDI
Class IActive
Mohs Mouse/Rabbit PolyDetector Plus DAB HRP Brown BSB-0355-50
FDA UDI
Class IActive
Tween 20 100 ml
FDA UDI
Class IActive
Mart-1/Melan A control slides Control Slides, 5
FDA UDI
Class IActive
PIN MultiDetector (CK 34BE12, p63 & AMACR) BSB-0352-50
FDA UDI
Class IActive
Tinto Varicella Zoster Virus (SG1, SG1-1, SG2-2E6, SG3, SG4, NCP-1 & IE-62) BSB-3810-3-ASR
FDA UDI
Class IActive
CD79a Control Slides BSB-9111-CS
FDA UDI
Class IActive
Melanosome HMB-45 control slides Control Slides, 5
FDA UDI
Class IActive
Myelin Basic Protein RPab Concentrate, 0.1 ml
FDA UDI
Class IActive
FOXA1 / HNF-3A control slides Control Slides, 5
FDA UDI
Class IActive
Slide Label Roll (8, 000) labels BSB-7451
FDA UDI
Class IActive
IgG4 control slides Control Slides, 5
FDA UDI
Class IActive
Follicular Dendritic Cell control slides Control Slides, 5
FDA UDI
Class IActive
VEGF RMab Concentrate, 1 ml
FDA UDI
Class IActive
Adenovirus MMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Mouse/Rabbit ImmunoDetector HRP Label Ready-to-use, 200 ml
FDA UDI
Class IActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.