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 83 of 111
DeviceModel / ReferenceRegistriesClassStatus
TintoFast NGFR, BSB-18, MMab BSB-3696-15
EUDAMEDFDA UDI
IVD GeneralActive
PDX1, EP139, RMab BSB 3159
EUDAMEDFDA UDI
IVD GeneralActive
MiTF, C5 and D5, MMab BSB 6251
EUDAMEDFDA UDI
IVD GeneralActive
p40, ZR8, RMab BSB 2073
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD34, EP88, RMab BSB 6487
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Napsin A, EP205, RMab BSB 6990
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PAX-5, RBT-PAX5, RMab BSB 5863
EUDAMEDFDA UDI
IVD GeneralActive
PHOX2B, EP312, RMab BSB 3614
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Alpha Synuclein, BSB-114, MMab BSB 3287
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SOX-10, BSB-62, MMab BSB 2210
EUDAMEDFDA UDI
IVD GeneralActive
Herpes Simplex Virus II, BSB-116, MMab BSB 3467
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Actin Muscle Specific, HHF35, MMab BSB 5022
EUDAMEDFDA UDI
IVD GeneralActive
APOE4, BSB-170, MMab BSB-3798-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CTLA-4|CD152, RBT-CTLA-4, RMab BSB 3485
EUDAMEDFDA UDI
IVD GeneralActive
GATA3, EP368, RMab BSB 3333
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Prolactin, PRL02, MMab BSB 5891
EUDAMEDFDA UDI
IVD GeneralActive
bcl-2, EP36, RMab BSB 6544
EUDAMEDFDA UDI
IVD GeneralActive
Synaptophysin, Polyclonal, RPab BSB 5950
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Prame, RBT-PRAME, RMab BSB-3774-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PAX-2, EP235, RMab BSB 2567
EUDAMEDFDA UDI
IVD GeneralActive
CD163, 10D6, MMab BSB 6307
EUDAMEDFDA UDI
IVD GeneralActive
Tinto p63, EP174, RMab BSB 5849
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LIN28, EP150, RMab BSB 3562
EUDAMEDFDA UDI
IVD GeneralActive
LAG-3|CD223, EP294, RMab BSB 3366
EUDAMEDFDA UDI
IVD GeneralActive
IgM, Polyclonal, RPab BSB 3083
EUDAMEDFDA UDI
IVD GeneralActive
Tinto YAP1, BSB-146, MMab BSB-3755-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TMPRSS2, BSB-136, MMab BSB-3703-3
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Albumin, polyclonal, RPab BSB 3014
EUDAMEDFDA UDI
IVD GeneralActive
Progesterone Receptor, RBT-22, RMab BSB 5887
EUDAMEDFDA UDI
IVD GeneralActive
Chromogranin A, LK2H10, MMab BSB 5347
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C1q, Polyclonal, RPab BSB 3019
EUDAMEDFDA UDI
IVD GeneralActive
IgM, BSB-41, MMab BSB 5685
EUDAMEDFDA UDI
IVD GeneralActive
Tinto C4c|FITC, Polyclonal, RPab BSB-3003-15
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MLH1, RBT-MLH1, RMab BSB-3787-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TLE1, 1F5, MMab BSB 2314
EUDAMEDFDA UDI
IVD GeneralActive
Myosin Smooth Muscle, BSB-17, MMab BSB 5929
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CTLA-4|CD152, BSB-88, MMab BSB 2881
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Renal Cell Carcinoma, PN-15, MMab BSB 5911
EUDAMEDFDA UDI
IVD GeneralActive
CA19-9, 121SLE, MMab BSB 5111
EUDAMEDFDA UDI
IVD GeneralActive
CEA, BSB-13, MMab BSB 5341
EUDAMEDFDA UDI
IVD GeneralActive
Uroplakin III, Polyclonal, RPab BSB 2289
EUDAMEDFDA UDI
IVD GeneralActive
hCG, BSB-38, MMab BSB 5600
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD75, LN-1, MMab BSB 2721
EUDAMEDFDA UDI
IVD GeneralActive
Villin, EP163, RMab BSB 2305
EUDAMEDFDA UDI
IVD GeneralActive
Tinto bcl-2, BSB-5, MMab BSB 5071
EUDAMEDFDA UDI
IVD GeneralActive
SMAD4|DPC4, RBT-SMAD4, RMab BSB 3402
EUDAMEDFDA UDI
IVD GeneralActive
C4c, Polyclonal, RPab BSB 3037
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TAG-72, BSB-21, MMab BSB 5953
EUDAMEDFDA UDI
IVD GeneralActive
C4c|FITC, Polyclonal, RPab BSB-3003-1
EUDAMEDFDA UDI
IVD GeneralActive
CD57, BSB-10, MMab BSB 5278
EUDAMEDFDA UDI
IVD GeneralActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.