MedtechSourcebook

MEMRY CORPORATION

Contract manufacturer ยท Bethel, CT

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

2024Product codes first listed, by year (tallest: 4)2026
FDA registration
3004579081 (openFDA record; or search FDA's registration database)
FEI number
3004579081
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
Resonetics, LLC (FDA owner/operator no. 10078190)
Registered address
3 Berkshire Blvd, Bethel, CT 06801
Contract listings
9 device listings, 7 product codes, first listed Nov 8, 2024
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
EZBStylet For Catheter, Gastro-UrologyClass IGastroenterology and urologyContract manufacturingDec 26, 2024
HTNWasher, Bolt NutClass IIOrthopedicContract manufacturingNov 8, 2024
HTWBit, DrillClass IOrthopedicContract manufacturingMay 27, 2026
HWCScrew, Fixation, BoneClass IIOrthopedicContract manufacturingApr 15, 2025
JDRStaple, Fixation, BoneClass IIOrthopedicContract manufacturingNov 8, 2024
LXHOrthopedic Manual Surgical InstrumentClass IOrthopedicContract manufacturingJan 9, 2025
MBIFastener, Fixation, Nondegradable, Soft TissueClass IIOrthopedicContract manufacturingNov 8, 2024