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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 19 of 111| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Estrogen Receptor (RBT-11) | BSB 5496 (ASR) | FDA UDI | Class I | Active |
| FOXA1 RMab Control Slides | Control Slides, 5 | FDA UDI | Class I | Active |
| PolyDetector HRP Mulberry | BSB-0362-200 | FDA UDI | Class I | Active |
| Fast ChromoProtector | 100 ml | FDA UDI | Class I | Active |
| Thrombomodulin/ CD141 RMab | Concentrate, 0.5 ml | FDA UDI | Class I | Active |
| NGFR control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| CD146/MUC18/Mel-CAM, MMab | Concentrate, 0.5 ml | FDA UDI | Class I | Active |
| Cytokeratin 17 control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| INSM1 Control Slides | BSB-9246-CS | FDA UDI | Class I | Active |
| Tinto Granzyme B RPab | Predilute, 7 ml | FDA UDI | Class I | Active |
| Tinto HHV-8 (13B10) | BSB 5645 (ASR) | FDA UDI | Class I | Active |
| Ctla-4/Cd152 (rbt-Ctla-4) | BSB 3488 (ASR) | FDA UDI | Class I | Active |
| PGP 9.5 control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| PAX-6 RMab | Concentrate, 0.5 ml | FDA UDI | Class I | Active |
| Claudin 18.2 Control Slides | BSB-9451-CS | FDA UDI | Class I | Active |
| CD16 Control Slides | BSB-9073-CS | FDA UDI | Class I | Active |
| Tinto PSA MMab | Predilute, 15 ml | FDA UDI | Class I | Active |
| PolyDetector Alk Scarlet | 200 ml | FDA UDI | Class I | Active |
| ER/PR PolyDetector DAB HRP Brown | 150 tests | FDA UDI | Class I | Active |
| XyGreen PermaMounter | 100 ml | FDA UDI | Class I | Active |
| Tinto Helicobacter pylori (Polyclonal) | BSB 5605 (ASR) | FDA UDI | Class I | Active |
| MCM5 RMab | Concentrate, 0.1 ml | FDA UDI | Class I | Active |
| CDX2 Control Slides | BSB-9116-CS | FDA UDI | Class I | Active |
| BOB.1 Control Slides | BSB-9035-CS | FDA UDI | Class I | Active |
| Hemoglobin A RMab | Concentrate, 0.5 ml | FDA UDI | Class I | Active |
| MSH2 MMab | Concentrate, 0.1 ml | FDA UDI | Class I | Active |
| Tinto Cytokeratin 14, RMab | Predilute, 7 ml | FDA UDI | Class I | Active |
| Islet 1/ISL1 Control Slides | BSB-9248-CS | FDA UDI | Class I | Active |
| Claudin-7 Control Slides | BSB-9121-CS | FDA UDI | Class I | Active |
| MUC1 control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| Estrogen Receptor Control Slides | Control Slides, 5 | FDA UDI | Class I | Active |
| 3-core GIST Cell Line Microarray Control Slides | Control Slides, 5 | FDA UDI | Class I | Active |
| Mouse/Rabbit PolyDetector AP, w/ALK Scarlet | 50 ml | FDA UDI | Class I | Active |
| TCR Alpha Control Slides | BSB-9399-CS | FDA UDI | Class I | Active |
| NPM1/B23 Control Slides | BSB-9310-CS | FDA UDI | Class I | Active |
| Tinto SOX-11 (BSB-184) | BSB-3849-15 | FDA UDI | Class I | Active |
| Tinto BRAF V600E (RM8) | BSB 2824 (ASR) | FDA UDI | Class I | Active |
| 11-core Human Cancer TMA Control Slides | Control Slides, 5 | FDA UDI | Class I | Active |
| HLA-DR alpha chain Control Slides | BSB-9221-CS | FDA UDI | Class I | Active |
| Tinto Claudin 18.2 (RBT-CLDN18.2) | BSB-3835-7-ASR | FDA UDI | Class I | Active |
| Tinto Adenovirus (20/11 and 2/6) | BSB 5038 (ASR) | FDA UDI | Class I | Active |
| CD11c control slides | Control Slides, 5 | FDA UDI | Class I | Active |
| Maspin Control Slides | BSB-9267-CS | FDA UDI | Class I | Active |
| GFAP Control Slides | BSB-9194-CS | FDA UDI | Class I | Active |
| CD8 RMab Control Slides | Control Slides, 5 | FDA UDI | Class I | Active |
| Tinto CA-125 RMab | Predilute, 7 ml | FDA UDI | Class I | Active |
| Factor XIIIa Control Slides | Control Slides, 5 | FDA UDI | Class I | Active |
| C4d Control Slides | BSB-9045-CS | FDA UDI | Class I | Active |
| Tinto IgG, RPab | Predilute, 1 ml | FDA UDI | Class I | Active |
| TCR Beta Control Slides | Control Slides, 5 | FDA UDI | Class I | Active |
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