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 67 of 111
DeviceModel / ReferenceRegistriesClassStatus
MUM1, EP190, RMab BSB 6958
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Vimentin, EP21, RMab BSB 2309
EUDAMEDFDA UDI
IVD GeneralActive
CD123 IL-3Ra, BSB-59, MMab BSB 5328
EUDAMEDFDA UDI
IVD GeneralActive
Tinto c-Met|HGFR, EP1454Y, RMab BSB 6584
EUDAMEDFDA UDI
IVD GeneralActive
Progesterone Receptor, BSB-2, MMab BSB 2131
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD44, BSB-12, MMab BSB 6233
EUDAMEDFDA UDI
IVD GeneralActive
CD4, RBT-CD4, RMab BSB 5153
EUDAMEDFDA UDI
IVD GeneralActive
Tinto T-Bet|TBX-2, EP263, RMab BSB 2602
EUDAMEDFDA UDI
IVD GeneralActive
Cyclin D3, BSB-171, MMab BSB-3799-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Tryptase, G3, MMab BSB 5988
EUDAMEDFDA UDI
IVD GeneralActive
hPL, Polyclonal, RPab BSB 6804
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PRAME, RBT-PRAME, RMab BSB-2374-7
EUDAMEDFDA UDI
IVD GeneralActive
Myeloperoxidase, Polyclonal, RPab BSB 5790
EUDAMEDFDA UDI
IVD GeneralActive
Tinto LIN28, EP150, RMab BSB 3560
EUDAMEDFDA UDI
IVD GeneralActive
LH, BSB-53, MMab BSB 5727
EUDAMEDFDA UDI
IVD GeneralActive
IgG4, BSB-96, MMab BSB 6810
EUDAMEDFDA UDI
IVD GeneralActive
Kappa|FITC, Polyclonal, GPab BSB-3009-05
EUDAMEDFDA UDI
IVD GeneralActive
Claudin-5, EP224, RMab BSB 2403
EUDAMEDFDA UDI
IVD GeneralActive
Podoplanin|D2-40, D2-40, MMab BSB 6069
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Ki-67, EP5, RMab BSB 5709
EUDAMEDFDA UDI
IVD GeneralActive
Histone H3 Phospho, EP233, RMab BSB 2528
EUDAMEDFDA UDI
IVD GeneralActive
Fli-1, G146-222, MMab BSB 5522
EUDAMEDFDA UDI
IVD GeneralActive
CD34, QBEnd|10, MMab BSB 5229
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ALK-1|CD246, RBT-ALK1, RMab BSB 5045
EUDAMEDFDA UDI
IVD GeneralActive
CD147, BSB-137, MMab BSB-3704-1
EUDAMEDFDA UDI
IVD GeneralActive
CA-125, OC125, MMab BSB 5097
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SOX-10, BSB-62, MMab BSB 2211
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD2, AB75, MMab BSB 6207
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD33, RBT-CD33, RMab BSB 3448
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PAX-8, RM436, RMab BSB-3786-15
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast Androgen Receptor, BSB-4, MMab BSB-3690-7
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin HMW 34BE12, 34BetaE12, MMab BSB 5395
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Fibrinogen|FITC, Polyclonal, RPab BSB-3004-7
EUDAMEDFDA UDI
IVD GeneralActive
Neurofilament, 2F11, MMab BSB 5816
EUDAMEDFDA UDI
IVD GeneralActive
MyoD1, EP212, RMab BSB 6977
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD56, 123C3.D5, MMab BSB 5269
EUDAMEDFDA UDI
IVD GeneralActive
HEG1, SKM9-2, MMab BSB-3728-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Thyroid Peroxidase, EP159, RMab BSB 2615
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD142|TF|Coagulation Factor III, BSB-143, MMab BSB-3718-15
EUDAMEDFDA UDI
IVD GeneralActive
NKX3.1, EP356, RMab BSB 3116
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SOX-9, EP317, RMab BSB 3211
EUDAMEDFDA UDI
IVD GeneralActive
PAX-8, RM436, RMab BSB-3786-1
EUDAMEDFDA UDI
IVD GeneralActive
S100A1, EP184, RMab BSB 2164
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgG|FITC, Polyclonal, GPab BSB-3007-7
EUDAMEDFDA UDI
IVD GeneralActive
PRAME, RBT-PRAME, RMab BSB-2374-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PD-1|CD279, NAT-105, MMab BSB 6213
EUDAMEDFDA UDI
IVD GeneralActive
MUC4, 8G7, MMab BSB 2990
EUDAMEDFDA UDI
IVD GeneralActive
Retinoblastoma| Rb, 1F8, MMab BSB 6131
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Glucagon, BSB-111, MMab BSB 3343
EUDAMEDFDA UDI
IVD GeneralActive
CD68, BSB-8, MMab BSB 5291
EUDAMEDFDA UDI
IVD GeneralActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.