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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 35 of 111
DeviceModel / ReferenceRegistriesClassStatus
Hepatitis B Virus Surface Antigen (A10F1) BSB 5620 (ASR)
FDA UDI
Class IActive
Herpes Simplex Virus I (10A3) BSB 2689 (ASR)
FDA UDI
Class IActive
PolyDetector Alk Blue Ready-To-Use 50 ml
FDA UDI
Class IActive
Bcl-x RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
Tinto FOXO1 RMab Predilute, 15 ml
FDA UDI
Class IActive
pan-TRK (RM423) BSB-3742-01-ASR
FDA UDI
Class IActive
Cyclin D1 control slides Control Slides, 5
FDA UDI
Class IActive
SV40 (Pab101) BSB 2235 (ASR)
FDA UDI
Class IActive
T. cruzi (BSB-183) BSB-3838-1-ASR
FDA UDI
Class IActive
hCG Control Slides BSB-9202-CS
FDA UDI
Class IActive
Tinto Herpes Simplex Virus I (10A3) BSB 2686 (ASR)
FDA UDI
Class IActive
PolyDetector HRP Black kit 150 Tests
FDA UDI
Class IActive
Cytokeratin 5 RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Lambda Control Slides BSB-9254-CS
FDA UDI
Class IActive
CD42b Control Slides BSB-9092-CS
FDA UDI
Class IActive
Tinto TdT RPab Predilute, 7 ml
FDA UDI
Class IActive
Tinto Calcitonin, RPab Predilute, 3 ml
FDA UDI
Class IActive
MCM5 RMab Concentrate, 0.5 ml
FDA UDI
Class IActive
Myogenin control slides Control Slides, 5
FDA UDI
Class IActive
Herpes Simplex Virus II (BSB-116) BSB 3466 (ASR)
FDA UDI
Class IActive
ImmunoDNA Digestor 15 ml
FDA UDI
Class IActive
Tinto Histone H3 Phospho (RBT-pHH3) BSB-3844-15
FDA UDI
Class IActive
PiT1 (BSB-182) BSB-3837-05
FDA UDI
Class IActive
Cytokeratin 10 control slides Control Slides, 5
FDA UDI
Class IActive
Tinto Glucagon Predilute, 7 ml
FDA UDI
Class IActive
Actin Muscle Specific control slides Control Slides, 5
FDA UDI
Class IActive
Satb2 (rbt-Satb2) BSB-3848-05
FDA UDI
Class IActive
PD-1/CD279 control slides Control Slides, 5
FDA UDI
Class IActive
LEF-1 control slides Control Slides, 5
FDA UDI
Class IActive
B7H3/CD276 RMab Control slides Control Slides, 5
FDA UDI
Class IActive
p16 control slides Control Slides, 5
FDA UDI
Class IActive
SDHB Control Slides BSB-9376-CS
FDA UDI
Class IActive
S100Beta, RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Mohs Mouse/Rabbit PolyDetector HRP Green Detection System Kit, 100ml
FDA UDI
Class IActive
Tinto PD-L1/CD274 (28-8) BSB-2371-15-ASR
FDA UDI
Class IActive
MUC1 Control Slides BSB-9287-CS
FDA UDI
Class IActive
Calcitonin control slides Control Slides, 5
FDA UDI
Class IActive
CD57 control slides Control Slides, 5
FDA UDI
Class IActive
BRAF V600E control slides Control Slides, 5
FDA UDI
Class IActive
Tinto pan-TRK (RM423) BSB-3742-15-ASR
FDA UDI
Class IActive
Mouse/Rabbit PolyDetector AP Label Ready-to-use, 50 ml each
FDA UDI
Class IActive
Pink Hematoxylin Counterstainer BSB-0360-50
FDA UDI
Class IActive
S100A6 control slides Control Slides, 5
FDA UDI
Class IActive
HER2 neu Phospho RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Tinto Progesterone Receptor (BSB-2) BSB 2127 (ASR)
FDA UDI
Class IActive
Muc4 (rbt-Muc4) BSB-3841-01
FDA UDI
Class IActive
Calretinin RMab Concentrate, 0.1 ml
FDA UDI
Class IActive
Somatostatin Receptor 2/SSTR2 Control Slides BSB-9381-CS
FDA UDI
Class IActive
Tinto CA-125, RMab Predilute, 3 ml
FDA UDI
Class IActive
PSP94/MSMB Control Slides Control Slides, 5
FDA UDI
Class IActive

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