Contract manufacturerLYOPHILIZATION SERVICES OF NEW ENGLAND, INC. (Manchester, NH)New HampshireCardiovascularNeurologyGeneral and plastic surgeryOrthopedicClass IIUnclassifiedClass III
LYOPHILIZATION SERVICES OF NEW ENGLAND, INC.
Contract manufacturer · Manchester, NH
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 1225991 (openFDA record; or search FDA's registration database)
- FEI number
- 3002516348
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Lyophilization Services of New England, Inc. (FDA owner/operator no. 9031362)
- Registered address
- 1 Sundial Ave Ste 112, Manchester, NH 03103
- Contract listings
- 6 device listings, 6 product codes, first listed Jan 8, 2008
- 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 code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| DXC | Clamp, Vascular | Class II | Cardiovascular | Contract manufacturing | Jan 8, 2008 |
| GXQ | Dura Substitute | Class II | Neurology | Contract manufacturing | Jan 13, 2016 |
| KGN | Wound Dressing With Animal-Derived Material(S) | Unclassified | General and plastic surgery | Contract manufacturing | Dec 14, 2021 |
| LMF | Agent, Absorbable Hemostatic, Collagen Based | Class III | General and plastic surgery | Contract manufacturing | Jan 8, 2008 |
| MQV | Filler, Bone Void, Calcium Compound | Class II | Orthopedic | Contract manufacturing | Dec 15, 2015 |
| PSQ | Intracardiac Patch Or Pledget, Biologically Derived | Class II | Cardiovascular | Contract manufacturing | Dec 22, 2022 |