MedtechSourcebook

Vygon MFG

Contract manufacturer and sterilizer · Dover, NH

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

FDA registration
1223004 (openFDA record; or search FDA's registration database)
FEI number
1000120555
Registered for
FDA registration year 2026
Establishment types
Specification developer; Manufacturer; Contract manufacturer; Repackager or relabeler; Contract sterilizer
Owner or operator
VYGON USA (FDA owner/operator no. 2245270)
Registered address
87 Venture Dr, Dover, NH 03820
Contract listings
6 device listings, 5 product codes, first listed Jan 3, 2013
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
FMINeedle, Hypodermic, Single LumenClass IIGeneral hospitalContract manufacturingFeb 17, 2023
FPASet, Administration, IntravascularClass IIGeneral hospitalContract manufacturingJan 3, 2013
FPASet, Administration, IntravascularClass IIGeneral hospitalContract sterilizationJan 3, 2013
OJAIntravenous Extension Tubing SetClass IIGeneral hospitalContract manufacturingSep 7, 2016
OJAIntravenous Extension Tubing SetClass IIGeneral hospitalContract sterilizationSep 7, 2016
OXQDressing Change TrayClass IGeneral hospitalContract manufacturingJan 14, 2013
OXQDressing Change TrayClass IGeneral hospitalContract sterilizationJan 14, 2013
PXBPercutaneous Introducer KitClass IIGeneral hospitalContract manufacturingMar 26, 2018

Other contract facilities of VYGON USA