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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 100 of 111
DeviceModel / ReferenceRegistriesClassStatus
hPL, EP241, RMab BSB 2416
EUDAMEDFDA UDI
IVD GeneralActive
CD103|ITGAE, EP206, RMab BSB 2862
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MSH6, 44, MMab BSB 6143
EUDAMEDFDA UDI
IVD GeneralActive
bcl-10, BSB-22, MMab BSB 2702
EUDAMEDFDA UDI
IVD GeneralActive
Desmoglein-3, EP306, RMab BSB 2899
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Calcitonin, EP92, RMab BSB 6410
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Langerin, 12D6, MMab BSB 6844
EUDAMEDFDA UDI
IVD GeneralActive
Tinto hCG, BSB-38, MMab BSB 5598
EUDAMEDFDA UDI
IVD GeneralActive
SMAD4|DPC4, RBT-SMAD4, RMab BSB 3403
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Renal Cell Carcinoma, PN-15, MMab BSB 5910
EUDAMEDFDA UDI
IVD GeneralActive
OCT-4, EP143, RMab BSB 2033
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CDK4, EP180, RMab BSB 2463
EUDAMEDFDA UDI
IVD GeneralActive
BCOR, BSB-128, MMab BSB-2370-05
EUDAMEDFDA UDI
IVD GeneralActive
PAX-5, RBT-PAX5, RMab BSB 5864
EUDAMEDFDA UDI
IVD GeneralActive
Tinto EpCAM|Epithelial Specific Antigen, MOC-31, MMab BSB 6724
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TLE1, RBT-TLE1, RMab BSB-3794-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto YAP1, BSB-146, MMab BSB-3755-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD147, BSB-137, MMab BSB-3704-7
EUDAMEDFDA UDI
IVD GeneralActive
CXCR5|CD185, Polyclonal, RPab BSB-3721-05
EUDAMEDFDA UDI
IVD GeneralActive
BOB.1, RBT BOB.1, RMab BSB-3700-05
EUDAMEDFDA UDI
IVD GeneralActive
CD68, KP-1, MMab BSB 2717
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mesothelial Cell, HBME-1, MMab BSB 3457
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD31, 1A10, MMab BSB 5218
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MSH2, BSB-147, MMab BSB-3722-7
EUDAMEDFDA UDI
IVD GeneralActive
Fli-1, G146-222, MMab BSB 5524
EUDAMEDFDA UDI
IVD GeneralActive
TORC3|CRTC3, BSB-175, MMab BSB-3805-01
EUDAMEDFDA UDI
IVD GeneralActive
CD138, EP201, RMab BSB 6531
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Claudin-5, EP224, RMab BSB 2400
EUDAMEDFDA UDI
IVD GeneralActive
IDH1 R132H, RBT-IDH1, RMab BSB-3732-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Inhibin Alpha, R1, MMab BSB 5689
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SOX-10, EP268, RMab BSB 2581
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NSE, BSB-94, MMab BSB 5820
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Lambda, BSB-16, MMab BSB 5716
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD68, BSB-8, MMab BSB 5288
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Mammaglobin, EP249, RMab BSB 5743
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C3c|FITC, Polyclonal, RPab BSB-3002-3
EUDAMEDFDA UDI
IVD GeneralActive
NSE, BSB-94, MMab BSB 5824
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgA, Polyclonal, RPab BSB 3054
EUDAMEDFDA UDI
IVD GeneralActive
T-Bet|TBX-2, EP263, RMab BSB 2605
EUDAMEDFDA UDI
IVD GeneralActive
PTEN, RM265, RMab BSB-3769-01
EUDAMEDFDA UDI
IVD GeneralActive
MyoD1, EP212, RMab BSB 6978
EUDAMEDFDA UDI
IVD GeneralActive
MNDA, BSB-157, MMab BSB-3738-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Inhibin Alpha, R1, MMab BSB 5688
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Progesterone Receptor, EP2, RMab BSB 2573
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p57, Kp10, MMab BSB 6191
EUDAMEDFDA UDI
IVD GeneralActive
Actin Muscle Specific, HHF35, MMab BSB 5026
EUDAMEDFDA UDI
IVD GeneralActive
p16, 16P04, JC2, MMab BSB 5831
EUDAMEDFDA UDI
IVD GeneralActive
Uroplakin III, EP321, RMab BSB 3244
EUDAMEDFDA UDI
IVD GeneralActive
Collagen Type IV, CIV22, MMab BSB 5355
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PAX-8, ZR-1, RMab BSB 2099
EUDAMEDFDA UDI
IVD GeneralActive

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