FDA.report

NovoSource

FDA Registration(s)

RegistrationFEINameStatusInitial importerExpiration yearAddress
30142736443014273644NOVOSOURCE, LLC1N2026-01-011000 HAMPTON CTR STE A Morgantown WV US 26505

GUDID Contact Samples

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDIDProductPhoneEmail
00811382037658NovoHip Total Hip System - Cup Alignment Guide3045542167xx@xx.xx
00811382037672NovoKnee Total Knee System - Handle, Tibial Insert Impactor3045542167xx@xx.xx
00811382037689NovoHip Total Hip System - Biolox Ball Head, 36-12/14S3045542167xx@xx.xx
00811382037696NovoHip Total Hip System - Biolox Ball Head, 36-12/14M3045542167xx@xx.xx

Registered Device Listings

Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2156211426793987K140701NOVOHIP BIPOLAR HEAD/NOVOHIP VITAMIN E LINER/ BONE SCREWS/ HOLE PLUGOQG2014-06-27
2156211161105122K132158NOVOHIP TOTAL HIP SYSTEMLPH2014-02-21
2156212065094711K131398NOVOKNEE TOTAL KNEE SYSTEMJWH2013-09-16
2156211943986271K123339TK1 TOTAL KNEE SYSTEMJWH2013-04-11

Product Codes Associated With Registrations

Product codeRegistration listing recordsLatest decision
JWH22013-09-16
OQG12014-06-27
LPH12014-02-21

PMN

GUDID

200 records. Showing 1-40. Next