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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 81 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto Retinoblastoma| Rb, 1F8, MMab BSB 6128
EUDAMEDFDA UDI
IVD GeneralActive
Tinto BG8 LewisY, F3, MMab BSB 6375
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TIA-1, TIA-1, MMab BSB 6354
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ARID1A, EP303, RMab BSB-3749-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD20, L26, MMab BSB 5191
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD35, EP197, RMab BSB 6493
EUDAMEDFDA UDI
IVD GeneralActive
Mesothelial Cell, HBME-1, MMab BSB 3459
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Bax, E63, RMab BSB 6078
EUDAMEDFDA UDI
IVD GeneralActive
PSAP, PASE|4LJ, MMab BSB 5907
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ERCC1, EP219, RMab BSB 2482
EUDAMEDFDA UDI
IVD GeneralActive
CD19, BSB-97, MMab BSB 6231
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgG, BSB-40, MMab BSB 5673
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Granzyme B, EP230, RMab BSB 2405
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TSH, EP254, RMab BSB 2623
EUDAMEDFDA UDI
IVD GeneralActive
Bax, E63, RMab BSB 6082
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD21, EP64, RMab BSB 5198
EUDAMEDFDA UDI
IVD GeneralActive
EGFR Phospho, EP11, RMab BSB 6720
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD42b, EP409, RMab BSB 3504
EUDAMEDFDA UDI
IVD GeneralActive
Somatostatin Receptor 2|SSTR2, EP149, RMab BSB-3748-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto EpCAM|Epithelial Specific Antigen, Ber-EP4, MMab BSB 6275
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HER2 neu, EP3, RMab BSB 2512
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Adipophilin, BSB-91, MMab BSB-3772-15
EUDAMEDFDA UDI
IVD GeneralActive
CD15, BSB-119, MMab BSB 5186
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p14 ARF, RBT-p14, RMab BSB 3597
EUDAMEDFDA UDI
IVD GeneralActive
Tinto A-1-Antichymotrypsin, EP384, RMab BSB 3498
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FSH, EP257, RMab BSB 3540
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PAX-7, BSB-145, MMab BSB-3743-7
EUDAMEDFDA UDI
IVD GeneralActive
PAX-2, EP235, RMab BSB 2569
EUDAMEDFDA UDI
IVD GeneralActive
Survivin, EP119, RMab BSB 2227
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NGFR, BSB-18, MMab BSB 6291
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Carbonic Anhydrase 9, EP161, RMab BSB 6416
EUDAMEDFDA UDI
IVD GeneralActive
IL-6, BSB-140, MMab BSB-3707-05
EUDAMEDFDA UDI
IVD GeneralActive
S-100, 4C4.9, MMab BSB 5921
EUDAMEDFDA UDI
IVD GeneralActive
p21, DCS-60.2, MMab BSB 2066
EUDAMEDFDA UDI
IVD GeneralActive
GH, EP267, RMab BSB 2501
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast CK AE1 and AE3, AE1 and AE3, MMab BSB 3665
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Musashi 2, RM422, RMab BSB-3740-15
EUDAMEDFDA UDI
IVD GeneralActive
IgD, EP173, RMab BSB 2962
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IL-6, BSB-140, MMab BSB-3707-15
EUDAMEDFDA UDI
IVD GeneralActive
Nestin, EP287, RMab BSB 2004
EUDAMEDFDA UDI
IVD GeneralActive
IDH1 R132H, IHC132, MMab BSB 3551
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Amyloid A, EP335, RMab BSB 2804
EUDAMEDFDA UDI
IVD GeneralActive
CD75, LN-1, MMab BSB 2723
EUDAMEDFDA UDI
IVD GeneralActive
TLE1, BSB-142, MMab BSB-3784-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Gastrin, Polyclonal, RPab BSB 5548
EUDAMEDFDA UDI
IVD GeneralActive
PAX-8, ZR-1, RMab BSB 2102
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Candida Albicans, RBT-C.alb, RMab BSB-3803-7
EUDAMED
IVD GeneralActive
MSH6, 44, MMab BSB 6146
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NKX3.1, EP356, RMab BSB 3113
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Fumarate Hydratase|Fumarase, BSB-151, MMab BSB-3726-15
EUDAMEDFDA UDI
IVD GeneralActive

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