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NATIONAL DISTRIBUTION & CONTRACTING, INC.

Last updated May 24, 2026

What NATIONAL DISTRIBUTION & CONTRACTING, INC. makes

The company manufactures silicone-based dental impression materials for creating precise oral molds, single-use patient drapes for examination and treatment procedures, and sterilization packaging designed for one-time use. It also produces mechanical external stethoscopes for auscultation, transcutaneous electrical stimulation electrodes for therapeutic use, and non-antimicrobial skin-cover adhesive strips. Additionally, the portfolio includes aneroid manual sphygmomanometers for blood pressure measurement and dentifrice for oral hygiene, alongside dental sutures and adhesive strips for wound coverage.

The company’s products are classified under FDA regulations as either Class I or Class II devices and are listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for use in clinical, dental, and home healthcare settings, adhering to U.S. medical device compliance requirements. The manufacturer operates within the United States, aligning its offerings with domestic regulatory standards.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
Address: —
Website: ndc-inc.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 6153663225
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 009831413

Catalogue (463)

Page 6 of 10

Device	Model / Reference	Registries	Class	Status
Quala	QMH535-CSO	FDA UDI	Class I	Active
Quala	Q10050	FDA UDI	Class I	Active
Pro Advantage	P542015	FDA UDI	Class I	Active
Pro Advantage	P212100	FDA UDI	Class II	Active
Pro Advantage	P549515	FDA UDI	Class II	Active
Pro Advantage	P428695	FDA UDI	Class II	Active
Pro Advantage	P640951	FDA UDI	Class II	Active
Quala	Q-9002HP	FDA UDI	Class II	Active
Pro Advantage	P157118	FDA UDI	Class I	Active
Quala	ADC400R	FDA UDI	Class I	Active
Pro Advantage	P428698	FDA UDI	Class II	Active
Quala	200-380	FDA UDI	Class II	Active
Quala	P0422-3	FDA UDI	Class I	Active
Pro Advantage	P702020	FDA UDI	Class I	Active
Quala	P1029-7	FDA UDI	Class I	Active
Quala	Q-8020	FDA UDI	Class I	Active
Pro Advantage	P428661	FDA UDI	Class II	Active
Pro Advantage	P080014	FDA UDI	Class I	Active
Quala	32829C	FDA UDI	Class II	Active
Pro Advantage	P640855	FDA UDI	Class II	Active
Quala	Q10210	FDA UDI	Class I	Active
Pro Advantage	P640955	FDA UDI	Class II	Active
Pro Advantage	P542027	FDA UDI	Class I	Active
Pro Advantage	N407310	FDA UDI	Class I	Active
Quala	32827C	FDA UDI	Class II	Active
Quala	QNHMH	FDA UDI	Class I	Active
Quala	WPADCPDR	FDA UDI	Class I	Active
Pro Advantage	P421698	FDA UDI	Class II	Active
Quala	WPADCPAQ	FDA UDI	Class I	Active
Quala	QRBL45	FDA UDI	Class I	Active
Pro Advantage	N407125	FDA UDI	Class I	Active
Pro Advantage	P548440	FDA UDI	Class II	Active
Pro Advantage	P702010	FDA UDI	Class I	Active
Pro Advantage	P542017	FDA UDI	Class I	Active
Quala	QUIN-100030K	FDA UDI	Class II	Active
Quala	32829C	FDA UDI	Class II	Active
Quala	32828C	FDA UDI	Class II	Active
Quala	Q30149	FDA UDI	Class I	Active
Pro Advantage	P704115	FDA UDI	Class I	Active
Quala	32824C	FDA UDI	Class II	Active
Quala	P0411-3	FDA UDI	Class I	Active
Pro Advantage	P542210	FDA UDI	Class I	Active
Pro Advantage	P548380	FDA UDI	Class II	Active
Pro Advantage	P701010	FDA UDI	Class I	Active
Pro Advantage	P702015	FDA UDI	Class I	Active
Quala	QH3	FDA UDI	Class I	Active
Pro Advantage	P301115	FDA UDI	Class II	Active
Quala	QM510-SS4	FDA UDI	Class I	Active
Pro Advantage	P211050	FDA UDI	Class II	Active
Pro Advantage	P212050	FDA UDI	Class II	Active

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Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (2)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

National Distribution & Contracting, Inc. has two recall records, both initiated on August 24, 2021. The records are marked with open and classified statuses. Both involve ultrasound gels and lotions from Eco-Med Pharmaceutical, Inc., with the reason stated as potential bacterial contamination.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Aug 24, 2021	Z-0068-2022	—	open, classified	Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.
Aug 24, 2021	Z-0067-2022	—	open, classified	Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.