MedtechSourcebook

CDB CORPORATION

Contract manufacturer ยท Leland, NC

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

2016Product codes first listed, by year (tallest: 1)2026
FDA registration
1054415 (openFDA record; or search FDA's registration database)
FEI number
3003069616
Registered for
FDA registration year 2026
Establishment types
Complaint file establishment; Specification developer; Manufacturer; Contract manufacturer; Repackager or relabeler
Owner or operator
CDB CORP. (FDA owner/operator no. 9002860)
Registered address
8770 Trade Street, Suite A, Leland, NC 28451
Contract listings
2 device listings, 2 product codes, first listed Apr 13, 2016
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
DYWBracket, Plastic, OrthodonticClass IIDentalContract manufacturingApr 13, 2016
NJMBracket, Ceramic, OrthodonticClass IIDentalContract manufacturingDec 2, 2019