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