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NATIONAL DISTRIBUTION & CONTRACTING, INC.

US

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
—
Phone
6153663225
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
009831413

Catalogue (463)

Page 5 of 10
DeviceModel / ReferenceRegistriesClassStatus
Quala 18201-QU
FDA UDI
Class IActive
Quala QF23
FDA UDI
Class IActive
Quala GCIBLA
FDA UDI
Class IIActive
Quala 689400
FDA UDI
Class IIActive
Quala WPADCPLV
FDA UDI
Class IActive
Quala AD2790
FDA UDI
Class IIActive
Quala Q602330
FDA UDI
Class IIActive
Pro Advantage 76200
FDA UDI
Class IIActive
Quala QNHHB
FDA UDI
Class IActive
Quala Suture Silk P00072
FDA UDI
Class IIActive
Pro Advantage P421666
FDA UDI
Class IIActive
Quala QH4
FDA UDI
Class IActive
Pro Advantage P211150
FDA UDI
Class IIActive
Pro Advantage N407030
FDA UDI
Class IActive
Quala WPAPAAQ
FDA UDI
Class IActive
Quala P0410-3
FDA UDI
Class IIActive
Quala 200-376
FDA UDI
Class IIActive
Pro Advantage P642000
FDA UDI
Class IIActive
Pro Advantage N207100
FDA UDI
Class IIActive
Quala Q17802
FDA UDI
Class IActive
Quala Q-9004HP
FDA UDI
Class IIActive
Pro Advantage P542007
FDA UDI
Class IActive
Quala QUIN-100025K
FDA UDI
Class IIActive
Quala QM520-CS5
FDA UDI
Class IActive
Quala QF151
FDA UDI
Class IActive
Quala 32823C
FDA UDI
Class IIActive
Quala 32825C
FDA UDI
Class IIActive
Pro Advantage P157116
FDA UDI
Class IActive
Pro Advantage P159544
FDA UDI
Class IActive
Pro Advantage P703020
FDA UDI
Class IIActive
Quala WPAPAPE
FDA UDI
Class IActive
Quala GCPKA
FDA UDI
Class IIActive
Pro Advantage P012790
FDA UDI
Class IIActive
Pro Advantage N407300
FDA UDI
Class IActive
Pro Advantage P640953
FDA UDI
Class IIActive
Pro Advantage P420635
FDA UDI
Class IIActive
Pro Advantage P150145
FDA UDI
Class IActive
Pro Advantage P704110
FDA UDI
Class IActive
Quala LAD3590
FDA UDI
Class IIActive
Quala WEADCEBG
FDA UDI
Class IActive
Pro Advantage N407525
FDA UDI
Class IActive
Pro Advantage P542141
FDA UDI
Class IActive
Quala 689410
FDA UDI
Class IIActive
Pro Advantage P750333
FDA UDI
Class IActive
Pro Advantage P150125
FDA UDI
Class IActive
Quala LAD2790
FDA UDI
Class IIActive
Pro Advantage P230023
FDA UDI
Class IActive
Pro Advantage N407145
FDA UDI
Class IActive
Quala Q85805
FDA UDI
Class IIActive
Pro Advantage P420684
FDA UDI
Class IIActive

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.

DateRecall No.ClassStatusReason
Aug 24, 2021Z-0068-2022—open, classified

Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.

Aug 24, 2021Z-0067-2022—open, classified

Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.