Protech Leaded Eyewear Inc

FDA Filings

This page includes the latest FDA filings for Protech Leaded Eyewear Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number1063300
FEI Number1000488948
NamePROTECH LEADED EYEWEAR, INC.
Owner & OperatorProtech Leaded Eyewear, Inc.
Contact Address1360 N Killian Dr Ste 2
Lake Park FL 33403 US
Official Correspondent
  • Christian Knighton
  • x-561-6279769-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1360 N Killian Dr Ste 2
Lake Park, FL 33403 US
Establishment Type
  • Repack or Relabel Medical Device
  • Develop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
PROTECH LEADED EYEWEAR, INC.
Proguard Isolation Gowns2020-04-19
PROTECH LEADED EYEWEAR, INC.
Proguard Protective Mask2020-04-19
PROTECH LEADED EYEWEAR, INC.
Proguard Leader2018-12-21
PROTECH LEADED EYEWEAR, INC.
Fit Over2018-12-21
PROTECH LEADED EYEWEAR, INC.
Face Shield2018-12-21
PROTECH LEADED EYEWEAR, INC.
Comet2018-12-21
PROTECH LEADED EYEWEAR, INC.
Astroflex2018-12-21
PROTECH LEADED EYEWEAR, INC.
9941 Ultralite2018-12-21
PROTECH LEADED EYEWEAR, INC.
9935 Ultralite2018-12-21
PROTECH LEADED EYEWEAR, INC.
99 Ultralite2018-12-21
PROTECH LEADED EYEWEAR, INC.
99 Alumilite2018-12-21
PROTECH LEADED EYEWEAR, INC.
53 Wrap2018-12-21
PROTECH LEADED EYEWEAR, INC.
Protech Leaed Eyewear Inc.2008-04-14
PROTECH LEADED EYEWEAR, INC.
Protex2008-04-14
PROTECH LEADED EYEWEAR, INC.
ProGuard Elite2008-04-14
PROTECH LEADED EYEWEAR, INC.
ProGuard Brand2008-04-14
PROTECH LEADED EYEWEAR, INC.
Protective Apron2008-04-14
PROTECH LEADED EYEWEAR, INC.
Proguard Radiation Reducing Sleeve2008-04-14

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