FDA Device Entity Profile: CONMED CORPORATION

Known Identifiers & Locations

FEI Numbers 1000305720, 1017294, 3001451571, 3004491689, 3007305485, 3019101334

Owner Operator Numbers 1317214

Locations Covered Chihuahua, MX; Greenwood Village, CO, US; LARGO, FL, US; New Haven, CT, US; Utica, NY, US; WESTBOROUGH, MA, US

Registered Establishments (6)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
1017294	Linvatec Corporation	LARGO, FL, US	Manufacture Medical Device	View Details
1223925	Conmed Corporation	WESTBOROUGH, MA, US	Develop Specifications But Do Not Manufacture At This Facility	View Details
1320894	CONMED CORPORATION	Utica, NY, US	Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device	View Details
3004491689	ConMed Corporation	Greenwood Village, CO, US	Develop Specifications But Do Not Manufacture At This Facility	View Details
3007305485	Consolidated Medical Equipment Company	Chihuahua, MX	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
3019101334	ConMed Corporation	New Haven, CT, US	Develop Specifications But Do Not Manufacture At This Facility	View Details

510(k) Premarket Notifications (1)

Submission #	Device Name	Decision Date	Decision Description	Action
K193606	Y-Knot OneStep Anchor	2020-01-22	Substantially Equivalent	View Details

FDA Recall History (0)

No recall records found for this entity.

Profile Disclaimer

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