Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

RESOURCE OPTIMIZATION & INNOVATION, L.L.C.

US

Last updated May 23, 2026

What RESOURCE OPTIMIZATION & INNOVATION, L.L.C. makes

The company manufactures single-use protective apparel and medical accessories, including isolation gowns, scrub suits, and surgical gowns designed for healthcare settings. It also produces disposable electrode conductive skin pads, stockinette, arterial blood sampling kits, and woven gauze pads for wound care. Additionally, the portfolio includes single-use blood pressure cuffs for clinical monitoring.

The devices fall under FDA Class I, Class II, and Unclassified (U) regulatory categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States and adheres to applicable U.S. medical device regulations.

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 Resource Optimization & Innovation, L.L.C. manufacture?

Resource Optimization & Innovation, L.L.C. specializes in single-use medical devices primarily for healthcare settings. Their portfolio includes protective apparel like isolation gowns, scrub suits, and surgical gowns, as well as accessories such as disposable electrode conductive skin pads, stockinette, arterial blood sampling kits, woven gauze pads (non-antimicrobial), and single-use blood pressure cuffs. These products are designed for clinical use, patient safety, and procedural efficiency.

Where is Resource Optimization & Innovation, L.L.C. based?

The company is headquartered in the United States. While the specific location isn’t detailed, its operations and regulatory compliance align with U.S. medical device standards, including FDA requirements.

Which regulatory registries or databases list the devices made by Resource Optimization & Innovation, L.L.C.?

The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers and regulators, allowing them to identify and verify specific devices through standardized identifiers.

How are the devices manufactured by Resource Optimization & Innovation, L.L.C. classified under FDA regulations?

The devices fall into three regulatory classifications: Class I (generally low-risk devices requiring general controls), Class II (moderate-risk devices needing special controls), and Unclassified (U) for those not yet assigned a risk category. Classification depends on factors like intended use, potential risks, and patient exposure, as determined by FDA guidelines.

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

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
945020902

Catalogue (1170)

Page 10 of 24
DeviceModel / ReferenceRegistriesClassStatus
Regard™ UN 401
FDA UDI
Class IActive
Regard™ OB0548
FDA UDI
Class IIUnknown
Regard™ GS0703
FDA UDI
Class IIUnknown
Regard™ EY0916
FDA UDI
Class IIUnknown
Regard™ CV0494
FDA UDI
Class IIUnknown
Regard™ OR0690
FDA UDI
Class IUnknown
Regard™ ET1030
FDA UDI
Class IUnknown
Regard™ CV0364
FDA UDI
Class IIUnknown
Regard™ GS0359
FDA UDI
Class IIUnknown
Regard™ OR0021
FDA UDI
Class IUnknown
Regard™ LD0269
FDA UDI
Class IIUnknown
Regard™ GS0420
FDA UDI
Class IIUnknown
Regard™ CV0634
FDA UDI
Class IIUnknown
Regard™ EY0448
FDA UDI
Class IIUnknown
Regard™ OR0977
FDA UDI
Class IUnknown
Regard™ OR0351
FDA UDI
Class IUnknown
Regard™ GY0811
FDA UDI
Class IIUnknown
Regard™ CHMG53GNS800XL-REG
FDA UDI
Class IActive
Regard™ UR0050
FDA UDI
Class IIUnknown
Regard™ CV0190
FDA UDI
Class IIUnknown
Regard™ OR0675
FDA UDI
Class IUnknown
Regard™ GY0502
FDA UDI
Class IIUnknown
Regard™ GS0782
FDA UDI
Class IIUnknown
Regard™ GS0832
FDA UDI
Class IUnknown
Regard™ NU1001
FDA UDI
Class IUnknown
Regard™ CV0820
FDA UDI
Class IIUnknown
Regard™ GU0664
FDA UDI
Class IIUnknown
Regard™ GS0724
FDA UDI
Class IIUnknown
Regard™ A3SRGST4X-REG
FDA UDI
Class IIActive
Regard™ DRP1-15X15ST-REG
FDA UDI
Class IIActive
Regard™ CV0283
FDA UDI
Class IIUnknown
Regard™ ORTWLBLDX6-REG
FDA UDI
Class IActive
Regard™ LD0056
FDA UDI
Class IIUnknown
Regard™ OR0601
FDA UDI
Class IUnknown
Regard™ PL0380
FDA UDI
Class IUnknown
Regard™ OB0102
FDA UDI
Class IIUnknown
Regard™ HT0016
FDA UDI
Class IIUnknown
Regard™ GS0466
FDA UDI
Class IIUnknown
Regard™ OR0969
FDA UDI
Class IUnknown
Regard™ GS0757
FDA UDI
Class IIUnknown
Regard™ LD0554
FDA UDI
Class IIUnknown
Regard™ GY0941
FDA UDI
Class IIUnknown
Regard™ GY0485
FDA UDI
Class IIUnknown
Regard™ CV0079
FDA UDI
Class IIUnknown
Regard™ LD0019
FDA UDI
Class IIUnknown
Regard™ OR0049
FDA UDI
Class IUnknown
Regard™ GS0307
FDA UDI
Class IIUnknown
Regard™ LD0652
FDA UDI
Class IIUnknown
Regard™ UR0098
FDA UDI
Class IIUnknown
Regard™ OR0320
FDA UDI
Class IUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.