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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 86 of 111
DeviceModel / ReferenceRegistriesClassStatus
Treponema pallidum, Polyclonal, RPab BSB 3236
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GATA3, EP368, RMab BSB 3329
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CTLA-4|CD152, BSB-88, MMab BSB 2880
EUDAMEDFDA UDI
IVD GeneralActive
Tryptase, G3, MMab BSB 5990
EUDAMEDFDA UDI
IVD GeneralActive
GCDFP-15, 23A3, MMab BSB 5558
EUDAMEDFDA UDI
IVD GeneralActive
MUC1, RBT-MUC1, RMab BSB-3788-1
EUDAMEDFDA UDI
IVD GeneralActive
Arginase-1, EP261, RMab BSB 2451
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PDX1, EP139, RMab BSB 3156
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Caveolin-1, EP353, RMab BSB 3316
EUDAMEDFDA UDI
IVD GeneralActive
CD35, RLB25, MMab BSB 5235
EUDAMEDFDA UDI
IVD GeneralActive
TCR Beta, BSB-117, MMab BSB 2262
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C1q|FITC, Polyclonal, RPab BSB-3001-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Claudin-7, EP399, RMab BSB-3719-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin 17, BSB-33, MMab BSB 2727
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FOXL2, Polyclonal, RPab BSB-3725-15
EUDAMEDFDA UDI
IVD GeneralActive
TLE1, BSB-142, MMab BSB-3784-05
EUDAMEDFDA UDI
IVD GeneralActive
Cytokeratin 20, EP23, RMab BSB 6705
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Stathmin, EP247, RMab BSB 2596
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IFN-Alpha, BSB-158, MMab BSB-3733-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto OX-40|CD134, BSB-90, MMab BSB 3120
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Lambda|FITC, Polyclonal, GPab BSB-3010-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CA-125, OC125, MMab BSB 5094
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TFE3, EP285, RMab BSB 3226
EUDAMEDFDA UDI
IVD GeneralActive
ICOS|CD278, RM417, RMab BSB-3731-05
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast HMB-45, HMB-45, MMab BSB-3693-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto hPL, Polyclonal, RPab BSB 6800
EUDAMEDFDA UDI
IVD GeneralActive
Tyrosinase, BSB-6, MMab BSB 6013
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IL-1a, BSB-138, MMab BSB-3705-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Somatostatin, BSB-113, MMab BSB 3413
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD79a, JCB117, MMab BSB 5303
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cathepsin K, BSB-172, MMab BSB-3800-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cyclin B1, RM281, RMab BSB-3760-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD38, SPC32, MMab BSB 6199
EUDAMEDFDA UDI
IVD GeneralActive
Tinto S-100, 4C4.9, MMab BSB 5918
EUDAMEDFDA UDI
IVD GeneralActive
Carbonic Anhydrase 9, EP161, RMab BSB 6420
EUDAMEDFDA UDI
IVD GeneralActive
SDHB, BSB-131, MMab BSB-2375-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto INSM1, RBT-INSM1, RMab BSB-3780-15
EUDAMEDFDA UDI
IVD GeneralActive
Estrogen Receptor, RBT-11, RMab BSB 5496
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast HMB-45, HMB-45, MMab BSB-3693-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ROS-1, EP282, RMab BSB 3623
EUDAMEDFDA UDI
IVD GeneralActive
C4d, EP272, RMab BSB 2836
EUDAMEDFDA UDI
IVD GeneralActive
MCM2, RBT-MCM2, RMab BSB 6334
EUDAMEDFDA UDI
IVD GeneralActive
NKX3.1, EP356, RMab BSB 3117
EUDAMEDFDA UDI
IVD GeneralActive
Tinto DOG-1, RBT-DOG1, RMab BSB 6268
EUDAMEDFDA UDI
IVD GeneralActive
Tinto HEG1, SKM9-2, MMab BSB-3728-3
EUDAMEDFDA UDI
IVD GeneralActive
CD163, 10D6, MMab BSB 6308
EUDAMEDFDA UDI
IVD GeneralActive
OX-40|CD134, BSB-90, MMab BSB 3125
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SV40, Pab101, MMab BSB 2231
EUDAMEDFDA UDI
IVD GeneralActive
PAX-8, ZR-1, RMab BSB 2103
EUDAMEDFDA UDI
IVD GeneralActive
CD25, RBT-CD25, RMab BSB 2457
EUDAMEDFDA UDI
IVD GeneralActive

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