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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 1 of 10
DeviceModel / ReferenceRegistriesClassStatus
Pro Advantage P017513
FDA UDI
Class IIActive
Pro Advantage P548210
FDA UDI
Class IIActive
Pro Advantage P080018
FDA UDI
Class IIActive
Pro Advantage P548200
FDA UDI
Class IIActive
Quala Gut Plain Suture P00810
FDA UDI
Class IIActive
Quala Q-8021
FDA UDI
Class IActive
Pro Advantage P542035
FDA UDI
Class IActive
Pro Advantage P428683
FDA UDI
Class IIActive
Pro Advantage P640952
FDA UDI
Class IIActive
Quala Q40253
FDA UDI
Class IIActive
Pro Advantage P548330
FDA UDI
Class IIActive
Quala WPAPAGR
FDA UDI
Class IActive
Pro Advantage P420496
FDA UDI
Class IIActive
Pro Advantage P428699
FDA UDI
Class IIActive
Pro Advantage P703025
FDA UDI
Class IIActive
Quala QF150
FDA UDI
Class IActive
Quala Q055026
FDA UDI
Class IIActive
Pro Advantage P640854
FDA UDI
Class IIActive
Quala Q602452
FDA UDI
Class IIActive
Pro Advantage P154010
FDA UDI
Class IActive
Pro Advantage N407420
FDA UDI
Class IActive
Quala Q589512
FDA UDI
Class IIActive
Pro Advantage P080010
FDA UDI
Class IActive
Pro Advantage P640853
FDA UDI
Class IIActive
Pro Advantage P153010
FDA UDI
Class IActive
Quala QS17
FDA UDI
Class IActive
Quala P0413-3
FDA UDI
Class IActive
Pro Advantage P548340
FDA UDI
Class IIActive
Pro Advantage P850091
FDA UDI
Class IIActive
Quala P0441-3
FDA UDI
Class IActive
Quala Q-9003HP
FDA UDI
Class IIActive
Pro Advantage P015410
FDA UDI
Class IIActive
Quala Q16990
FDA UDI
Class IActive
Pro Advantage P157022
FDA UDI
Class IActive
Quala Q40252
FDA UDI
Class IIActive
Pro Advantage P151020
FDA UDI
Class IActive
Pro Advantage 76100
FDA UDI
Class IActive
Quala QRF30
FDA UDI
Class IActive
Pro Advantage P542025
FDA UDI
Class IActive
Quala Q48060
FDA UDI
Class IActive
Quala QUIN-10025K
FDA UDI
Class IIActive
Pro Advantage P158020
FDA UDI
Class IActive
Quala AD2440
FDA UDI
Class IIActive
Pro Advantage P850098
FDA UDI
Class IIActive
Pro Advantage P542022
FDA UDI
Class IActive
Pro Advantage N407002
FDA UDI
Class IActive
Quala Q-9001HP
FDA UDI
Class IIActive
Pro Advantage P301105
FDA UDI
Class IIActive
Pro Advantage P012424
FDA UDI
Class IIActive
Quala Q30610
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.