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 34 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto Beta-Catenin, RMab Predilute, 3 ml
FDA UDI
Class IActive
TintoMixing Station Kit BSB-7453
FDA UDI
Class IActive
hGAL / GCET2 control slides Control Slides, 5
FDA UDI
Class IActive
PRAME Control Slides BSB-9351-CS
FDA UDI
Class IActive
PolyDetector Liquid DAB HRP Brown kit 1000 tests
FDA UDI
Class IActive
Cytokeratin 5 & 6 & ERG RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
B7h3/Cd276 (rbt-B7h3) BSB 2815 (ASR)
FDA UDI
Class IActive
Pd-L1/Cd274 (rbt-Pdl1) BSB 2653 (ASR)
FDA UDI
Class IActive
pTau Phospho/Thr 181 Control Slides BSB-9445-CS
FDA UDI
Class IActive
c-Myc Control Slides BSB-9040-CS
FDA UDI
Class IActive
CD41/Integrin alpha IIb Control Slides BSB-9091-CS
FDA UDI
Class IActive
Parvovirus Control Slides Control Slides, 5
FDA UDI
Class IActive
MyoD1 (RBT-MYOD1) BSB-3829-05
FDA UDI
Class IActive
Tinto Cytokeratin 5 & 14 RMab Predilute, 7 ml
FDA UDI
Class IActive
Tinto S100A8/MRP8, RMab Predilute, 15 ml
FDA UDI
Class IActive
p27 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Cytokeratin 5 & 6, RMab Predilute, 15 ml
FDA UDI
Class IActive
Tinto Detector CapGap Plus Slides BSB 7006
FDA UDI
Class IActive
Tinto PAX-6 RMab Predilute, 15 ml
FDA UDI
Class IActive
Cd16 (rbt-Cd16) BSB-3842-01
FDA UDI
Class IActive
PolyDetector HRP Fuchsia BSB-0364-100
FDA UDI
Class IActive
PolyDetector Alk Red Ready-To-Use 50 ml
FDA UDI
Class IActive
Tinto Hepatitis B Virus Core Antigen, RPab Predilute, 7 ml
FDA UDI
Class IActive
Tinto Cytokeratin HMW AE3, MMab Predilute, 3 ml
FDA UDI
Class IActive
Tinto T-Bet/TBX-2 RMab Control Slides Control Slides, 5
FDA UDI
Class IActive
Tinto Adenovirus, MMab Predilute, 7 ml
FDA UDI
Class IActive
Tinto Thyroglobulin, RMab Predilute, 7 ml
FDA UDI
Class IActive
Calretinin (RBT-CALB2) BSB-3815-05
FDA UDI
Class IActive
Villin Control Slides BSB-9427-CS
FDA UDI
Class IActive
Rabbit FluoroDetector FITC with FluoroMounter 15 ml
FDA UDI
Class IActive
Cd16 (rbt-Cd16) BSB-3842-05
FDA UDI
Class IActive
CD11c Control Slides BSB-9063-CS
FDA UDI
Class IActive
Tinto Estrogen Receptor (RBT-11) BSB 5493 (ASR)
FDA UDI
Class IActive
PU.1 Control Slides BSB-9361-CS
FDA UDI
Class IActive
STAT6 Control Slides BSB-9389-CS
FDA UDI
Class IActive
Tinto Myelin Basic Protein, RMab Predilute, 3 ml
FDA UDI
Class IActive
Ros-1 (ep282) BSB 3628 (ASR)
FDA UDI
Class IActive
Tinto PSA MMab Predilute, 3 ml
FDA UDI
Class IActive
Tinto Adenovirus (20/11 and 2/6) BSB 5037 (ASR)
FDA UDI
Class IActive
EGFR controol slides Control Slides, 5
FDA UDI
Class IActive
IgG4 control slides Control Slides, 5
FDA UDI
Class IActive
CA-125 RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
MUC2 Control Slides Control Slides, 5
FDA UDI
Class IActive
Mycobacterium tuberculosis Control Slides BSB-9294-CS
FDA UDI
Class IActive
PolyDetector HRP Black kit 5000 Tests
FDA UDI
Class IActive
Desmin RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
TintoReagent Container used with tube 6mL BSB-7456
FDA UDI
Class IActive
Granzyme B RPab Concentrate, 0.5 ml
FDA UDI
Class IActive
Tinto Cyclin D1, RMab Predilute, 7 ml
FDA UDI
Class IActive
MUC1 control slides Control Slides, 5
FDA UDI
Class IActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.