Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Bosma Enterprises

US

Last updated May 24, 2026

What Bosma Enterprises makes

Bosma Enterprises manufactures single-use surgical and examination gloves, including polyisoprene, hevea-latex, polychloroprene, and nitrile varieties, all non-powdered and non-antimicrobial. Their portfolio also includes surgical linen/cushion sets, operating room turnover kits, limb/torso/head restraints, and bucket liners designed for medical and procedural use.

The company’s products are regulated under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identification (UDI) database. The manufacturer is based in 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 Bosma Enterprises manufacture?

Bosma Enterprises specializes in single-use medical devices primarily for surgical and examination settings. Their portfolio includes non-powdered, non-antimicrobial gloves made from materials like polyisoprene, hevea-latex, polychloroprene, and nitrile. They also produce surgical linen/cushion sets, operating room turnover kits, limb/torso/head restraints, and bucket liners. These products are designed to meet procedural and surgical needs while adhering to regulatory standards.

Where is Bosma Enterprises based, and how does that affect its devices?

Bosma Enterprises is based in the United States, which means its devices are subject to FDA regulations. The company’s products fall under FDA’s Class I and Class II categories, indicating varying levels of regulatory oversight depending on the device’s risk profile. Being U.S.-based also means compliance with domestic manufacturing and safety standards, ensuring alignment with FDA requirements for device authorization.

Which regulatory registries or databases list Bosma Enterprises’ devices?

Bosma Enterprises’ devices are listed in the FDA’s Unique Device Identification (UDI) database. The UDI system helps track and identify medical devices throughout their lifecycle, ensuring transparency in the supply chain and regulatory compliance. Listing in this database is a requirement for devices marketed in the U.S., including those manufactured by Bosma Enterprises.

How are Bosma Enterprises’ devices classified under FDA regulations?

Bosma Enterprises’ devices are classified under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential harm, and regulatory history, as outlined in FDA guidelines.

Why do some of Bosma Enterprises’ devices appear under different brand names like Biogel or Gammex?

Some of Bosma Enterprises’ devices may be distributed or marketed under different brand names like Biogel or Gammex due to licensing agreements, private-label contracts, or distribution partnerships. These brands represent the same manufacturer but cater to specific market segments or customer preferences. The underlying product design, materials, and regulatory compliance remain consistent with Bosma Enterprises’ standards.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
bosma.org
LinkedIn
—
Facebook
—
Phone
800-362-5463
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
878070325

Catalogue (509)

Page 6 of 11
DeviceModel / ReferenceRegistriesClassStatus
Biogel 71-30655
FDA UDI
Class IActive
Encore 71-5785003
FDA UDI
Class IActive
Biogel 71-31470
FDA UDI
Class IActive
Biogel 71-ML42675
FDA UDI
Class IActive
Gammex 71-AN77280
FDA UDI
Class IActive
Bosma Enterprises 10-8020SDO
FDA UDI
Class IActive
Triumph 71-ME2380
FDA UDI
Class IUnknown
Biogel 71-ML48955
FDA UDI
Class IActive
Ambu 10-601177-1
FDA UDI
Class IIActive
Biogel 71-31060
FDA UDI
Class IActive
Gammex 71-AN86590
FDA UDI
Class IActive
Good Works 72-50401
FDA UDI
Class IActive
Protexis 71-CR2LS70
FDA UDI
Class IActive
Gammex 71-AN85970
FDA UDI
Class IActive
Bosma Enterprises 10-8020A
FDA UDI
Class IActive
SensiCare 71-ME9070
FDA UDI
Class IActive
Biogel 71-40690
FDA UDI
Class IActive
Biogel 71-30690
FDA UDI
Class IActive
Gammex 71-AN87260
FDA UDI
Class IActive
Bosma Enterprises 10-8020COO
FDA UDI
Class IActive
Protexis 71-2D72PT70
FDA UDI
Class IActive
Gammex 71-AN85960
FDA UDI
Class IActive
Biogel 71-ML42165
FDA UDI
Class IActive
Biogel 71-30555
FDA UDI
Class IActive
Bosma Enterprises 10-8020HUL
FDA UDI
Class IActive
SensiCare 71-ME9075
FDA UDI
Class IActive
Biogel 71-82555
FDA UDI
Class IActive
Good Works 72-50602
FDA UDI
Class IActive
SensiCare 71-ME9490
FDA UDI
Class IActive
Bosma Enterprises 10-8020ALO
FDA UDI
Class IActive
Protexis 71-CR2PL85X
FDA UDI
Class IActive
SensiCare 71-ME9275
FDA UDI
Class IActive
Bosma Enterprises 10-7225
FDA UDI
Class IActive
Bosma Enterprises 10-8020B
FDA UDI
Class IActive
Biogel 71-31465
FDA UDI
Class IActive
Bosma Enterprises 10-8020MRO
FDA UDI
Class IActive
Bosma Enterprises 10-8020LR
FDA UDI
Class IActive
Biogel 71-ML48965
FDA UDI
Class IActive
Gammex 71-AN88265
FDA UDI
Class IActive
Good Works 72-50602
FDA UDI
Class IUnknown
Gammex 71-AN77265
FDA UDI
Class IActive
Biogel 71-30490
FDA UDI
Class IActive
Good Works 72-50601
FDA UDI
Class IActive
Protexis 71-CR3PM60
FDA UDI
Class IActive
Biogel 71-ML42685
FDA UDI
Class IActive
Biogel 71-30675
FDA UDI
Class IActive
Triumph 71-ME2355
FDA UDI
Class IUnknown
Gammex 71-AN85965
FDA UDI
Class IActive
Good Works 72-50603
FDA UDI
Class IUnknown
Biogel 71-ML42180
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.