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Sign in to claim this brandBIO 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
- —
- —
- [email protected]
- Phone
- +1(800)561-1145
- PRRC Contact
- Jessica Dunston
- EUDAMED SRN
- US-MF-000036462
- FDA FEI Number
- 3008773547
- DUNS Number
- 102855447
Catalogue (5547)
Page 17 of 111| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CD137/TNFRSF9 Control Slides | BSB-9066-CS | FDA UDI | Class I | Active |
| Tinto Estrogen Receptor (RBT-11) | BSB 5492 (ASR) | FDA UDI | Class I | Active |
| DOG-1 Control Slides | BSB-9163-CS | FDA UDI | Class I | Active |
| Nkx6.1 (rbt-Nkx6.1) | BSB-3836-1 | FDA UDI | Class I | Active |
| Tinto VEGFA (RBT-VEGFA) | BSB-3825-3 | FDA UDI | Class I | Active |
| Cytokeratin 7 & CDX2 RMab | Concentrate, 0.1 ml | FDA UDI | Class I | Active |
| CD61 control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| Tinto Somatostatin, RMab | Predilute, 15 ml | FDA UDI | Class I | Active |
| CD10 RMab | Concentrate, 1 ml | FDA UDI | Class I | Active |
| Ros-1 (ep282) | BSB 3627 (ASR) | FDA UDI | Class I | Active |
| Helicobacter Pylori control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| Cadherin-6, RMab | Concentrate, 0.1 ml | FDA UDI | Class I | Active |
| Tinto Myoglobin, RPab | Predilute, 7 ml | FDA UDI | Class I | Active |
| CTLA4 control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| Alpha-Fetoprotein RMab | Concentrate, 1 ml | FDA UDI | Class I | Active |
| Glut1 (rbt-Glut1) | BSB-3824-05 | FDA UDI | Class I | Active |
| Tinto CD10 (RBT-CD10) | BSB-3816-15 | FDA UDI | Class I | Active |
| Pygopus 2/Pygo 2 Control Slides | BSB-9362-CS | FDA UDI | Class I | Active |
| Factor XIIIa Control Slides | BSB-9176-CS | FDA UDI | Class I | Active |
| Tinto CD13 RMab | Predilute, 3 ml | FDA UDI | Class I | Active |
| CA-125 RMab | Concentrate, 1 ml | FDA UDI | Class I | Active |
| Tinto MUC4 (RBT-MUC4) | BSB-3841-7 | FDA UDI | Class I | Active |
| PolyDetector HRP Mulberry | BSB-0362-1000 | FDA UDI | Class I | Active |
| CD3 control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| IgG, RPab | Concentrate, 0.5 ml | FDA UDI | Class I | Active |
| Tinto Cytomegalovirus (8B1.2, 1G5.2 & 2D4.2) | BSB 5449 (ASR) | FDA UDI | Class I | Active |
| HER2 neu control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| TintoDetector Incubator | BSB 7002 | FDA UDI | Class I | Active |
| NSE control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| bcl-6 Control Slides | BSB-9030-CS | FDA UDI | Class I | Active |
| Cytokeratin 5 & 6 RMab | Concentrate, 0.1 ml | FDA UDI | Class I | Active |
| Cytomegalovirus MMab | Concentrate, 0.5 ml | FDA UDI | Class I | Active |
| Tinto Cytokeratin 5 & 6, RMab | Predilute, 3 ml | FDA UDI | Class I | Active |
| Myoglobin control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| Tinto Cytomegalovirus (8B1.2, 1G5.2 & 2D4.2) | BSB 5450 (ASR) | FDA UDI | Class I | Active |
| CD7 Control Slides | Control Slides, 5 | FDA UDI | Class I | Active |
| TintoReagent Tube with Cap 6mL | BSB-7455 | FDA UDI | Class I | Active |
| Granzyme B RPab | Concentrate, 0.1 ml | FDA UDI | Class I | Active |
| Cytokeratin 5 & 6 (RM341) | BSB-3822-1 | FDA UDI | Class I | Active |
| Progesterone Receptor (BSB-2) | BSB 2130 (ASR) | FDA UDI | Class I | Active |
| Calretinin (RBT-CALB2) | BSB-3815-1 | FDA UDI | Class I | Active |
| OCT-2 Control Slides | BSB-9314-CS | FDA UDI | Class I | Active |
| Annexin VII Control Slides | BSB-9018-CS | FDA UDI | Class I | Active |
| Insulin RMab | Concentrate, 0.1 ml | FDA UDI | Class I | Active |
| Tinto ROS-1 (EP282) | BSB 3625 (ASR) | FDA UDI | Class I | Active |
| CD42b control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| PolyDetector HRP Blue Plus | BSB-0363-50 | FDA UDI | Class I | Active |
| Tinto pan-TRK (RBT-TRK) | BSB-2376-15-ASR | FDA UDI | Class I | Active |
| Treponema TMA, Artificial (2-core: Positive and Negative) Control Slides | Control Slides, 5 | FDA UDI | Class I | Active |
| Glucagon control slides | Control Slides, 5 | FDA UDI | Class I | Active |
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