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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 7 of 10
DeviceModel / ReferenceRegistriesClassStatus
Quala Q16793
FDA UDI
Class IActive
Pro Advantage P150155
FDA UDI
Class IActive
Pro Advantage P542121
FDA UDI
Class IActive
Pro Advantage P752023
FDA UDI
Class IActive
Pro Advantage P371000
FDA UDI
Class IActive
Quala P0431-3
FDA UDI
Class IActive
Quala Suture Chromic Gut P00525
FDA UDI
Class IIActive
Pro Advantage P420663
FDA UDI
Class IIActive
Pro Advantage P157025
FDA UDI
Class IActive
Pro Advantage P542030
FDA UDI
Class IActive
Quala Q40254
FDA UDI
Class IIActive
Quala Q10770
FDA UDI
Class IActive
Quala WPAPALV
FDA UDI
Class IActive
Quala 32823C
FDA UDI
Class IIActive
Quala QUIN-10030K
FDA UDI
Class IIActive
Quala Q-9005HP
FDA UDI
Class IIActive
Quala P1029
FDA UDI
Class IActive
Pro Advantage 76800
FDA UDI
Class IActive
Pro Advantage P640851
FDA UDI
Class IIActive
Quala QUIN-1030K
FDA UDI
Class IIActive
Pro Advantage P150160
FDA UDI
Class IActive
Quala Q48034
FDA UDI
Class IActive
Quala 18635-QU
FDA UDI
Class IActive
Quala ADC400F
FDA UDI
Class IActive
Pro Advantage P080021
FDA UDI
Class IIActive
Quala 32828C
FDA UDI
Class IIActive
Quala Q10780
FDA UDI
Class IActive
Quala silk suture P00064
FDA UDI
Class IIActive
Pro Advantage P157114
FDA UDI
Class IActive
Pro Advantage P929025
FDA UDI
Class IIActive
Quala WEADCEBL
FDA UDI
Class IActive
Pro Advantage P542202
FDA UDI
Class IActive
Pro Advantage P542002
FDA UDI
Class IActive
Pro Advantage P548450
FDA UDI
Class IIActive
Quala 200-360
FDA UDI
Class IIActive
Pro Advantage P542206
FDA UDI
Class IActive
Quala WPAPAWH
FDA UDI
Class IActive
Quala Q-9004HP
FDA UDI
Class IIActive
Pro Advantage P072522
FDA UDI
Class IActive
Pro Advantage P157117
FDA UDI
Class IActive
Quala Q48037
FDA UDI
Class IActive
Quala Q85803
FDA UDI
Class IIActive
Pro Advantage P850093
FDA UDI
Class IIActive
Pro Advantage P157024
FDA UDI
Class IActive
Pro Advantage P420497
FDA UDI
Class IIActive
Pro Advantage N407020
FDA UDI
Class IActive
Pro Advantage N407135
FDA UDI
Class IActive
Quala AD5410
FDA UDI
Class IIActive
Quala QMH536-CSR
FDA UDI
Class IActive
Quala Q10010
FDA UDI
Class IActive

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.