Nypro Inc (Maple Grove)
Maple Grove, MN, US
Nypro Inc (Maple Grove) appears in FDA device records in Maple Grove, MN. FDA records list no 510(k) clearances, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
- 510(k) clearances
- 0
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 1
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3011024991 | 3011024991 | Nypro Inc (Maple Grove) | 11400 73rd Ave N Ste 100, Maple Grove, MN 55369 US | 2026 | and 30 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
- HRXArthroscope
- HTWBit, Drill
- GFABlade, Saw, General & Plastic Surgery, Surgical
- GFFBur, Surgical, General & Plastic Surgery
- IKDCable, Electrode
- GEJCarrier, Ligature
- DRFCatheter, Electrode Recording, Or Probe, Electrode Recording
- NLGCatheter, Intracardiac Mapping, High-Density, Reprocessed
- NLHCatheter, Recording, Electrode, Reprocessed
- FZOChisel, Surgical, Manual
- NMJClip, Implantable, Reprocessed
- HWWCountersink
- ERLDrill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- NUJElectrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
- NLUForceps, Biopsy, Electric, Reprocessed
- NONForceps, Biopsy, Non-Electric, Reprocessed
- HDAForceps, Obstetrical
- GDZHandle, Scalpel
- HCFInstrument, Ligature Passing And Knot Tying
- MDMInstrument, Manual, Surgical, General Use
- HWEInstrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
- LFLInstrument, Ultrasonic Surgical
- DYBIntroducer, Catheter
- JYOKnife, Ear
- HTSKnife, Orthopedic
- GCJLaparoscope, General & Plastic Surgery
- NLMLaparoscope, General & Plastic Surgery, Reprocessed
- KMIMonitor, Bed Patient
- LXHOrthopedic Manual Surgical Instrument
- NLFOximeter, Reprocessed
- NDMPin, Fixation, Threaded, Metallic
- QNWReprocessed Bronchoscope
- PNEReprocessed Catheter Introducer
- OWQReprocessed Intravascular Ultrasound Catheter
- GADRetractor
- NLQSingle-Use Reprocessed Ultrasonic Surgical Instruments
- JOWSleeve, Limb, Compressible
- HWXTap, Bone
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
