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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 3 of 10
DeviceModel / ReferenceRegistriesClassStatus
Pro Advantage P850090
FDA UDI
Class IIActive
Quala Q2030
FDA UDI
Class IActive
Quala WEADCEDR
FDA UDI
Class IActive
Pro Advantage P750303
FDA UDI
Class IActive
Pro Advantage P420493
FDA UDI
Class IIActive
Quala Suture Silk P00071
FDA UDI
Class IIActive
Pro Advantage P150140
FDA UDI
Class IActive
Pro Advantage P428697
FDA UDI
Class IIActive
Quala GCILVA
FDA UDI
Class IIActive
Quala WPADCPWH
FDA UDI
Class IActive
Pro Advantage P701025
FDA UDI
Class IActive
Quala 18235-QU
FDA UDI
Class IActive
Pro Advantage P211099
FDA UDI
Class IIActive
Pro Advantage P212000
FDA UDI
Class IIActive
Quala QF88R
FDA UDI
Class IActive
Pro Advantage P428684
FDA UDI
Class IIActive
Quala 32821C
FDA UDI
Class IIActive
Pro Advantage P753023
FDA UDI
Class IActive
Pro Advantage P150110
FDA UDI
Class IActive
Pro Advantage N407560
FDA UDI
Class IActive
Quala 32822C
FDA UDI
Class IIActive
Quala QH2
FDA UDI
Class IActive
Pro Advantage N099001
FDA UDI
Class IIActive
Pro Advantage P420661
FDA UDI
Class IIActive
Pro Advantage P072523
FDA UDI
Class IActive
Pro Advantage N407215
FDA UDI
Class IActive
Quala QSCGC
FDA UDI
Class IActive
Quala P0440-3
FDA UDI
Class IActive
Quala 32826C
FDA UDI
Class IIActive
Pro Advantage P159522
FDA UDI
Class IActive
Quala WEADCEDR
FDA UDI
Class IActive
Pro Advantage P301008
FDA UDI
Class IIActive
Quala Q48033
FDA UDI
Class IActive
Pro Advantage 76900
FDA UDI
Class IActive
Quala Q48032
FDA UDI
Class IActive
Pro Advantage P542010
FDA UDI
Class IActive
Quala 200-390
FDA UDI
Class IIActive
Quala Q602448
FDA UDI
Class IIActive
Quala Q-9001HP
FDA UDI
Class IIActive
Quala P0442-3
FDA UDI
Class IActive
Quala Q17804
FDA UDI
Class IActive
Quala Q85806
FDA UDI
Class IIActive
Quala QF150S
FDA UDI
Class IActive
Pro Advantage P542029
FDA UDI
Class IActive
Quala Q10420
FDA UDI
Class IActive
Pro Advantage P012020
FDA UDI
Class IIActive
Quala OCA
FDA UDI
Class IIActive
Pro Advantage N099002
FDA UDI
Class IIActive
Pro Advantage P420698
FDA UDI
Class IIActive
Pro Advantage P150115
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.