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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
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Facebook
—
Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
945020902

Catalogue (1170)

Page 1 of 24
DeviceModel / ReferenceRegistriesClassStatus
Regard™ SP1063
FDA UDI
Class IIUnknown
Regard™ GS0917
FDA UDI
Class IIUnknown
Regard™ HT0495
FDA UDI
Class IIUnknown
Regard™ T100AC
FDA UDI
Class IIActive
Regard™ CHMG38GNS800M-REG
FDA UDI
Class IActive
Regard™ ABGALN1CC-REG
FDA UDI
Class IActive
Regard™ A4ISOP2XLNS-REG
FDA UDI
Class IIActive
Regard™ OR1044
FDA UDI
Class IUnknown
Regard™ ET0648
FDA UDI
Class IUnknown
Regard™ OB0287
FDA UDI
Class IIUnknown
Regard™ GU0700
FDA UDI
Class IIUnknown
Regard™ GS0823
FDA UDI
Class IIUnknown
Regard™ OR0529
FDA UDI
Class IUnknown
Regard™ DBPLGADLTL-REG
FDA UDI
Class IIActive
Regard™ DSPSCRBPNTM-REG
FDA UDI
Class IActive
Regard™ STKIMP9X48ST-REG
FDA UDI
Class IActive
Regard™ UR0746
FDA UDI
Class IIUnknown
Regard™ OR0319
FDA UDI
Class IUnknown
Regard™ OR0594
FDA UDI
Class IUnknown
Regard™ CV0755
FDA UDI
Class IIUnknown
Regard™ OR0749
FDA UDI
Class IUnknown
Regard™ 243449
FDA UDI
Class IIActive
Regard™ GS0816
FDA UDI
Class IIUnknown
Regard™ LD0756
FDA UDI
Class IIUnknown
Regard™ GS0706
FDA UDI
Class IIUnknown
Regard™ LD0108
FDA UDI
Class IIUnknown
Regard™ GS0853
FDA UDI
Class IIUnknown
Regard™ OR0949
FDA UDI
Class IUnknown
Regard™ GS0173
FDA UDI
Class IIUnknown
Regard™ 361094
FDA UDI
Class IIActive
Regard™ 236168
FDA UDI
Class IActive
Regard™ SHCVR2XL3-REG
FDA UDI
Class IActive
Regard™ NTRLCHMGLVS1-REG
FDA UDI
Class IActive
Regard™ CV0851
FDA UDI
Class IIUnknown
Regard™ A3SRGSTSM-REG
FDA UDI
Class IIActive
Regard™ OR0452
FDA UDI
Class IUnknown
Regard™ OR0208
FDA UDI
Class IUnknown
Regard™ HT1091
FDA UDI
Class IIUnknown
Regard™ GU1035
FDA UDI
Class IIUnknown
Regard™ C100LOAC-PHILIPS
FDA UDI
Class IIActive
Regard™ GS0752
FDA UDI
Class IIUnknown
Regard™ HT0334
FDA UDI
Class IIUnknown
Regard™ EY0236
FDA UDI
Class IIUnknown
Regard™ OR0583
FDA UDI
Class IUnknown
Regard™ OR0347
FDA UDI
Class IUnknown
Regard™ OB0230
FDA UDI
Class IIUnknown
Regard™ LD0186
FDA UDI
Class IIUnknown
Regard™ GS0087
FDA UDI
Class IIUnknown
Regard™ OR0785
FDA UDI
Class IUnknown
Regard™ 315674REG
FDA UDI
Class IActive

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