Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 77 of 111
DeviceModel / ReferenceRegistriesClassStatus
Tinto PELP1, RBT-PELP1, RMab BSB-3744-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IDH1 R132H, RBT-IDH1, RMab BSB-3732-3
EUDAMEDFDA UDI
IVD GeneralActive
p63, EP174, RMab BSB 5852
EUDAMEDFDA UDI
IVD GeneralActive
TSH, EP254, RMab BSB 2625
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PGP 9.5, BSB-46, MMab BSB 2114
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HER-2 neu, RBT-HER2, RMab BSB 2037
EUDAMEDFDA UDI
IVD GeneralActive
Herpes Simplex Virus I, 10A3, MMab BSB 2687
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgG, BSB-40, MMab BSB 5674
EUDAMEDFDA UDI
IVD GeneralActive
Fibrinogen, Polyclonal, RPab BSB 3052
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MSH2, BSB-147, MMab BSB-3722-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD23, EP75, RMab BSB 6471
EUDAMEDFDA UDI
IVD GeneralActive
Factor XIIIa, EP292, RMab BSB 5510
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Parafibromin, BSB-50, MMab BSB 2749
EUDAMEDFDA UDI
IVD GeneralActive
T-Bet|TBX-2, EP263, RMab BSB 2604
EUDAMEDFDA UDI
IVD GeneralActive
PU.1, EP18, RMab BSB 2158
EUDAMEDFDA UDI
IVD GeneralActive
Tinto iNOS, RBT-iNOS, RMab BSB 2656
EUDAMEDFDA UDI
IVD GeneralActive
Tinto NKX3.1, EP356, RMab BSB 3115
EUDAMEDFDA UDI
IVD GeneralActive
Synaptophysin, EP158, RMab BSB 2242
EUDAMEDFDA UDI
IVD GeneralActive
Cyclin B1, RM281, RMab BSB-3760-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgD|FITC, Polyclonal, GPab BSB-3006-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto pTau Phospho|Thr 181, BSB-176, MMab BSB-3807-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD30, Ber-H2, MMab BSB 5213
EUDAMEDFDA UDI
IVD GeneralActive
INI-1, 25, MMab BSB 6831
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PLAP, EP194, RMab BSB 5870
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Fli-1, G146-222, MMab BSB 5520
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p63, EP174, RMab BSB 5850
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Macrophage HAM-56, HAM-56, MMab BSB 5737
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Granzyme B, EP230, RMab BSB 2406
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin LMW CAM5.2, CAM5.2, MMab BSB 2058
EUDAMEDFDA UDI
IVD GeneralActive
Tinto T-Bet|TBX-2, EP263, RMab BSB 2603
EUDAMEDFDA UDI
IVD GeneralActive
TLE1, RBT-TLE1, RMab BSB-3794-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Caldesmon, BSB-19, MMab BSB 6099
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PDGFR-B, RBT-PDGFRB, RMab BSB 2349
EUDAMEDFDA UDI
IVD GeneralActive
Insulin, BSB-42, MMab BSB 5698
EUDAMEDFDA UDI
IVD GeneralActive
Aurora B, RM278, RMab BSB-3712-1
EUDAMEDFDA UDI
IVD GeneralActive
CD35, EP197, RMab BSB 6495
EUDAMEDFDA UDI
IVD GeneralActive
MUC6, CLH5, MMab BSB 6173
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD138, EP201, RMab BSB 6527
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Arginase-1, EP261, RMab BSB 2447
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HHV-8, 13B10, MMab BSB 5647
EUDAMEDFDA UDI
IVD GeneralActive
CD5, RBT-CD5, RMab BSB 5160
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Insulin, BSB-42, MMab BSB 5696
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Parvovirus, R92F6, MMab BSB 5856
EUDAMEDFDA UDI
IVD GeneralActive
INI-1, RBT-INI1, RMab BSB-3779-05
EUDAMEDFDA UDI
IVD GeneralActive
Glutamine Synthetase, GS-6, MMab BSB 2932
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Factor XIIIa, EP292, RMab BSB 5505
EUDAMEDFDA UDI
IVD GeneralActive
Tinto STAR, EP226, RMab BSB 3632
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD38, EP135, RMab BSB 6500
EUDAMEDFDA UDI
IVD GeneralActive
IgE|FITC, Polyclonal, GPab BSB-3011-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MLH1, RBT-MLH1, RMab BSB-3787-3
EUDAMEDFDA UDI
IVD GeneralActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.