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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 4 of 10

Device	Model / Reference	Registries	Class	Status
Pro Advantage	P549525	FDA UDI	Class II	Active
Quala	QM500-CS4	FDA UDI	Class I	Active
Pro Advantage	N407015	FDA UDI	Class I	Active
Pro Advantage	P150120	FDA UDI	Class I	Active
Quala	Q16995	FDA UDI	Class I	Active
Quala	Q055030	FDA UDI	Class II	Active
Pro Advantage	P420636	FDA UDI	Class II	Active
Pro Advantage	P250615	FDA UDI	Class I	Active
Pro Advantage	P548360	FDA UDI	Class II	Active
Quala	QS1	FDA UDI	Class I	Active
Quala	Q10917	FDA UDI	Class I	Active
Quala	Q-9006HP	FDA UDI	Class II	Active
Pro Advantage	P250550	FDA UDI	Class I	Active
Pro Advantage	P542111	FDA UDI	Class I	Active
Pro Advantage	P420422	FDA UDI	Class II	Active
Pro Advantage	P903200	FDA UDI	Class I	Active
Pro Advantage	P850089	FDA UDI	Class II	Active
Quala Suture Silk	P00065	FDA UDI	Class II	Active
Quala	QS18	FDA UDI	Class I	Active
Quala	P0421-3	FDA UDI	Class I	Active
Quala	Q589510	FDA UDI	Class II	Active
Quala	Q2030-7	FDA UDI	Class I	Active
Pro Advantage	P421667	FDA UDI	Class II	Active
Quala	QNHCW	FDA UDI	Class I	Active
Quala	Q16659	FDA UDI	Class I	Active
Quala	Q589510	FDA UDI	Class II	Active
Quala	AD3590	FDA UDI	Class II	Active
Pro Advantage	P211000	FDA UDI	Class II	Active
Quala Gut Plain Suture	P00822	FDA UDI	Class II	Active
Quala	Q10250	FDA UDI	Class I	Active
Pro Advantage	P548215	FDA UDI	Class II	Active
Quala	Q48059	FDA UDI	Class I	Active
Pro Advantage	N407200	FDA UDI	Class I	Active
Quala	WEADCEAQ	FDA UDI	Class I	Active
Pro Advantage	P420662	FDA UDI	Class II	Active
Pro Advantage	N407405	FDA UDI	Class I	Active
Quala	Q-9005HP	FDA UDI	Class II	Active
Pro Advantage	P929021	FDA UDI	Class II	Active
Pro Advantage	P549240	FDA UDI	Class II	Active
Quala	WPADCPPE	FDA UDI	Class I	Active
Pro Advantage	76700	FDA UDI	Class I	Active
Quala	Q400042ML	FDA UDI	Class II	Active
Quala	QM520-CS5	FDA UDI	Class I	Active
Pro Advantage	P080000	FDA UDI	Class I	Active
Quala	32824C	FDA UDI	Class II	Active
Pro Advantage	P420494	FDA UDI	Class II	Active
Quala	200-371-B	FDA UDI	Class I	Active
Quala	200-370-C	FDA UDI	Class I	Active
Pro Advantage	P150150	FDA UDI	Class I	Active
Quala	Q85802	FDA UDI	Class II	Active

Related Companies

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.