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 13 of 111
DeviceModel / ReferenceRegistriesClassStatus
Cyclin B1 RMab Concentrate, 1 ml
FDA UDI
Class IActive
Hemoglobin A RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
MCM5 Control Slides BSB-9270-CS
FDA UDI
Class IActive
HER-2 neu control slides Control Slides, 5
FDA UDI
Class IActive
CD73/NT5E Control Slides BSB-9108-CS
FDA UDI
Class IActive
c-Met/HGFR (RBT-c-Met/HGFR) BSB-3812-1
FDA UDI
Class IActive
NUT/NUTM1 Control Slides BSB-9313-CS
FDA UDI
Class IActive
Glucagon RPab Concentrate, 0.1 ml
FDA UDI
Class IActive
ImmunoDetector Protein Blocker / Antibody Diluent 50 ml
FDA UDI
Class IActive
Claudin-5 Control Slides Control Slides, 5
FDA UDI
Class IActive
CA15-3 Control Slides BSB-9047-CS
FDA UDI
Class IActive
Tinto Calretinin, RMab Predilute, 15 ml
FDA UDI
Class IActive
Fast ChromoProtector 1000 ml
FDA UDI
Class IActive
Alpha-Fetoprotein Control Slides BSB-9012-CS
FDA UDI
Class IActive
Tinto PSAP (RBT-PSAP) BSB-3846-15
FDA UDI
Class IActive
Mesothelin RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Glutamine Synthetase Control Slides BSB-9198-CS
FDA UDI
Class IActive
Tinto GCDFP-15, RMab Predilute, 3 ml
FDA UDI
Class IActive
PLAP Control Slides Control Slides, 5
FDA UDI
Class IActive
PolyDetector HRP Green kit 1000 Tests
FDA UDI
Class IActive
PolyDetector HRP Yellow BSB-0365-1000
FDA UDI
Class IActive
Tinto Histone H3 Phospho (RBT-pHH3) BSB-3844-7
FDA UDI
Class IActive
PolyDetector DAB HRP Brown Chromogen 6 ml
FDA UDI
Class IActive
Mesothelial Cell Control Slides BSB-9277-CS
FDA UDI
Class IActive
Herpes Simplex Virus I RPab Concentrate, 0.5 ml
FDA UDI
Class IActive
Cd4 (bsb-179) BSB-3818-01
FDA UDI
Class IActive
Mouse/Rabbit ImmunoDetector DAB HRP Brown Detection System 5 ml each
FDA UDI
Class IActive
GFAP RMab Concentrate, 1 ml
FDA UDI
Class IActive
Mohs Mouse/Rabbit PolyDetector Plus DAB HRP Brown BSB-0355-5
FDA UDI
Class IActive
c-Myc (RBT-CMYC) BSB-3813-05
FDA UDI
Class IActive
Spectrin RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Tinto Helicobacter Pylori (BSB-37) BSB 2677 (ASR)
FDA UDI
Class IActive
Follicular Dendritic Cell MMab Concentrate, 0.5 ml
FDA UDI
Class IActive
Carbonic Anhydrases 9 control slides Control Slides, 5
FDA UDI
Class IActive
VEGF RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Factor H/Complement Factor H Control Slides BSB-9174-CS
FDA UDI
Class IActive
Calcitonin RPab Concentrate, 1 ml
FDA UDI
Class IActive
Tinto EZH2 (RBT-EZH2) BSB-3823-15
FDA UDI
Class IActive
CD30 Control Slides BSB-9084-CS
FDA UDI
Class IActive
Braf V600e (rm8) BSB 2829 (ASR)
FDA UDI
Class IActive
PolyDetector HRP Yellow BSB-0365-15
FDA UDI
Class IActive
PolyDetector HRP Green kit 500 Tests
FDA UDI
Class IActive
B7h3/Cd276 (rbt-B7h3) BSB 2813 (ASR)
FDA UDI
Class IActive
Tinto Epstein Barr Virus LMP-1 (CS1-4) BSB 5484 (ASR)
FDA UDI
Class IActive
Tinto Cytokeratin 6, RMab Predilute, 15 ml
FDA UDI
Class IActive
CD163 Control Slides BSB-9074-CS
FDA UDI
Class IActive
Hepatitis B Virus Core Antigen Control Slides BSB-9207-CS
FDA UDI
Class IActive
Adenovirus (20/11 and 2/6) BSB 5041 (ASR)
FDA UDI
Class IActive
Clusterin/Apolipoprotein J (RM437) BSB-3821-01
FDA UDI
Class IActive
PHOX2B Control Slides BSB-9345-CS
FDA UDI
Class IActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.