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[[Image:fda-logo.jpg|right|thumb]]
The American Food and Drug Administration has approved several circumcision devices and products made from harvested infant foreskins.<ref name='fda-accucirc'>{{REFwebQuoteREFweb
| last=Brogdon
| first=Nancy C.
| work=
| date=2007-09-07
| urltitletitle=Dear Mr. Wallace
| url=http://www.accucirc.com/documents/AccuCirc_510k.pdf
| accessdate=2011-03-06
}}</ref><ref name='fda-dermagraft-tc'>{{REFwebQuoteREFweb
| quote=...fibroblast-derived temporary skin substitute for the treatment of partial-thickness burns that has been approved for marketing by the FDA.
| last=
| work=
| date=
| urltitletitle=Dermagraft-TC
| url=http://www.medilexicon.com/drugs/dermagraft-tc.php#GeneralInformation
| accessdate=
}}</ref><ref name='fda-apligraf'>{{REFwebQuoteREFweb
| quote=Apligraf® is the first bio-engineered cell based product to receive FDA approval (in 1998).
| last=
| work=
| date=
| urltitletitle=Apligraf
| url=http://www.organogenesis.com/products/bioactive_woundhealing/apligraf.html
| accessdate=2011-03-06
}}</ref><ref name='fda-alloderm'>{{REFwebQuoteREFweb
| quote=...screened and tested according to FDA regulations...
| last=
| work=
| date=
| urltitletitle=AlloDerm®Tissue Matrix defined
| url=http://www.lifecell.com/alloderm-regenerative-tissue-matrix/95/
| accessdate=2011-03-06