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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 2 of 10
DeviceModel / ReferenceRegistriesClassStatus
Pro Advantage N207105
FDA UDI
Class IIActive
Quala Q40255
FDA UDI
Class IIActive
Pro Advantage P548900
FDA UDI
Class IIActive
Quala WPADCPBL
FDA UDI
Class IActive
Quala QRBL30
FDA UDI
Class IActive
Pro Advantage 76801
FDA UDI
Class IActive
Pro Advantage P640954
FDA UDI
Class IIActive
Pro Advantage P420697
FDA UDI
Class IIActive
Quala WPADCPYE
FDA UDI
Class IActive
Quala LAD5410
FDA UDI
Class IIActive
Pro Advantage P157002
FDA UDI
Class IActive
Pro Advantage P158010
FDA UDI
Class IActive
Pro Advantage P157115
FDA UDI
Class IActive
Quala 32822C
FDA UDI
Class IIActive
Quala 32821C
FDA UDI
Class IIActive
Pro Advantage N407010
FDA UDI
Class IActive
Quala GCBLA
FDA UDI
Class IIActive
Pro Advantage P157004
FDA UDI
Class IActive
Quala Q602340
FDA UDI
Class IIActive
Pro Advantage P080023
FDA UDI
Class IIActive
Quala P1030-7
FDA UDI
Class IActive
Pro Advantage N407120
FDA UDI
Class IActive
Quala WEADCESI
FDA UDI
Class IActive
Quala WPADCPBG
FDA UDI
Class IActive
Quala P0412-3
FDA UDI
Class IActive
Pro Advantage N407225
FDA UDI
Class IActive
Pro Advantage N407205
FDA UDI
Class IActive
Pro Advantage P150130
FDA UDI
Class IActive
Pro Advantage P157112
FDA UDI
Class IActive
Quala 32827C
FDA UDI
Class IIActive
Quala Q30630
FDA UDI
Class IActive
Quala QF88L
FDA UDI
Class IActive
Pro Advantage P080028
FDA UDI
Class IIActive
Quala QMH537-SSO
FDA UDI
Class IActive
Pro Advantage P212150
FDA UDI
Class IActive
Pro Advantage N407035
FDA UDI
Class IActive
Quala WEADCELV
FDA UDI
Class IActive
Quala 18310-QU
FDA UDI
Class IActive
Quala Q055007
FDA UDI
Class IIActive
Quala QEHB3
FDA UDI
Class IActive
Pro Advantage P542131
FDA UDI
Class IActive
Quala Q40251
FDA UDI
Class IIActive
Pro Advantage P250200
FDA UDI
Class IIActive
Pro Advantage N407005
FDA UDI
Class IActive
Pro Advantage P150105
FDA UDI
Class IActive
Pro Advantage P754048
FDA UDI
Class IActive
Pro Advantage P072503
FDA UDI
Class IActive
Pro Advantage P542020
FDA UDI
Class IActive
Quala Q10902
FDA UDI
Class IActive
Pro Advantage P080016
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.