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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 9 of 10
DeviceModel / ReferenceRegistriesClassStatus
Pro Advantage P542204
FDA UDI
Class IActive
Quala QNHM
FDA UDI
Class IActive
Quala Q400122ML
FDA UDI
Class IIActive
Quala Q055022
FDA UDI
Class IIActive
Pro Advantage N407040
FDA UDI
Class IActive
Pro Advantage P159533
FDA UDI
Class IActive
Quala P0420-3
FDA UDI
Class IActive
Pro Advantage P542212
FDA UDI
Class IActive
Pro Advantage P154020
FDA UDI
Class IActive
Pro Advantage P080007
FDA UDI
Class IActive
Quala QUIN-1025K
FDA UDI
Class IIActive
Pro Advantage 77100
FDA UDI
Class IActive
Quala Q589512
FDA UDI
Class IIActive
Quala Nylon Suture P00662
FDA UDI
Class IIActive
Quala Q602335
FDA UDI
Class IIActive
Quala WEADCEPE
FDA UDI
Class IActive
Quala Chromic Gut Suture P00558
FDA UDI
Class IIActive
Quala GCIPKA
FDA UDI
Class IIActive
Quala Chromic Gut Suture P00635
FDA UDI
Class IIActive
Pro Advantage P152010
FDA UDI
Class IActive
Pro Advantage P154040
FDA UDI
Class IActive
Pro Advantage P080033
FDA UDI
Class IActive
Pro Advantage P150135
FDA UDI
Class IActive
Quala Q-9003HP
FDA UDI
Class IIActive
Pro Advantage P013554
FDA UDI
Class IIActive
Quala Suture Silk P00062
FDA UDI
Class IIActive
Pro Advantage P850096
FDA UDI
Class IIActive
Quala P1030
FDA UDI
Class IActive
Quala Q40012
FDA UDI
Class IIUnknown
Quala Q48058
FDA UDI
Class IActive
Pro Advantage P013590
FDA UDI
Class IIActive
Pro Advantage P420683
FDA UDI
Class IIActive
Quala 200-300
FDA UDI
Class IIActive
Pro Advantage P250300
FDA UDI
Class IIActive
Quala Q2029
FDA UDI
Class IActive
Quala WPAPASI
FDA UDI
Class IActive
Pro Advantage P211100
FDA UDI
Class IIActive
Quala Q9037
FDA UDI
Class IActive
Quala AD3554
FDA UDI
Class IIActive
Pro Advantage N407540
FDA UDI
Class IActive
Pro Advantage P640852
FDA UDI
Class IIActive
Quala Q40030
FDA UDI
Class IIActive
Quala 18410-QU
FDA UDI
Class IActive
Quala Q602412
FDA UDI
Class IIActive
Pro Advantage P701020
FDA UDI
Class IActive
Quala Q48035
FDA UDI
Class IActive
Pro Advantage P542012
FDA UDI
Class IActive
Pro Advantage P549260
FDA UDI
Class IIActive
Pro Advantage P542208
FDA UDI
Class IActive
Pro Advantage P151010
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.