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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 8 of 10

Device	Model / Reference	Registries	Class	Status
Pro Advantage	P250610	FDA UDI	Class I	Active
Pro Advantage	P158030	FDA UDI	Class I	Active
Quala	WPAPAYE	FDA UDI	Class I	Active
Quala Suture Plain Gut	P00592	FDA UDI	Class II	Active
Quala	Q85801	FDA UDI	Class II	Active
Quala	Q40004	FDA UDI	Class II	Unknown
Pro Advantage	P750003	FDA UDI	Class I	Active
Quala	Q2029-7	FDA UDI	Class I	Active
Pro Advantage	N407025	FDA UDI	Class I	Active
Quala	QEP9	FDA UDI	Class I	Active
Quala Suture Gut Chromic Suture	P00636	FDA UDI	Class II	Active
Quala	P0432-3	FDA UDI	Class I	Active
Pro Advantage	P211098	FDA UDI	Class II	Active
Pro Advantage	P371015	FDA UDI	Class I	Active
Pro Advantage	P154030	FDA UDI	Class I	Active
Pro Advantage	P549530	FDA UDI	Class II	Active
Quala	WEADCEWH	FDA UDI	Class I	Active
Pro Advantage	P158040	FDA UDI	Class I	Active
Pro Advantage	P548445	FDA UDI	Class II	Active
Quala	Q-9006HP	FDA UDI	Class II	Active
Pro Advantage	P701015	FDA UDI	Class I	Active
Pro Advantage	P929028	FDA UDI	Class II	Active
Pro Advantage	P549510	FDA UDI	Class II	Active
Quala	Q-9002HP	FDA UDI	Class II	Active
Quala	Q-9000HP	FDA UDI	Class II	Active
Pro Advantage	P541222	FDA UDI	Class II	Active
Quala	WEADCEYE	FDA UDI	Class I	Active
Pro Advantage	P420699	FDA UDI	Class II	Active
Pro Advantage	P549220	FDA UDI	Class II	Active
Quala Suture Silk	P00066	FDA UDI	Class II	Active
Quala	Q055003	FDA UDI	Class II	Active
Pro Advantage	P080063	FDA UDI	Class II	Active
Quala	QS9	FDA UDI	Class I	Active
Quala	32825C	FDA UDI	Class II	Active
Quala	QEP23	FDA UDI	Class I	Active
Pro Advantage	N407115	FDA UDI	Class I	Active
Pro Advantage	77000	FDA UDI	Class I	Active
Quala	Q-9000HP	FDA UDI	Class II	Active
Pro Advantage Buffered Iontophoresis Electrode Treatment Kit	P850325	FDA UDI	N/A	Active
Quala	Q40201	FDA UDI	Class II	Active
Quala	WPADCPGR	FDA UDI	Class I	Active
Pro Advantage	P072523	FDA UDI	Class I	Active
Pro Advantage	P072504	FDA UDI	Class I	Active
Quala	Q85804	FDA UDI	Class II	Active
Pro Advantage	P080095	FDA UDI	Class I	Active
Pro Advantage	P750013	FDA UDI	Class I	Active
Pro Advantage	P903100	FDA UDI	Class I	Active
Pro Advantage	P250100	FDA UDI	Class II	Active
Quala	Q30620	FDA UDI	Class I	Active
Pro Advantage	P157113	FDA UDI	Class I	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.