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PRECISION DYNAMICS CORPORATION

US

Last updated September 17, 2026

Information

Country
US
Address
25124 Springfield Ct Ste 200, Valencia, CA, 91355
Website
—
LinkedIn
—
Facebook
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Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
2020282
DUNS Number
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Catalogue (44)

DeviceModel / ReferenceRegistriesClassStatus
Duraholder Y5647879
FDA UDI
Class IActive
Comfort Cushion MCC002
FDA UDI
Class IActive
Gantry Guard Flex Mini CTG03
FDA UDI
Class IIUnknown
Gantry Guard SCTG01
FDA UDI
Class IIUnknown
Duraholder Y5647883
FDA UDI
Class IActive
Gantry Guard Flex CTG02
FDA UDI
Class IIUnknown
Pediatric Urine Collectors, Sterile 05002
FDA UDI
Class IActive
Duraholder Y5647878
FDA UDI
Class IActive
Pediatric Urine Collectors, Clean 05001
FDA UDI
Class IActive
UR-Assure 05001-00-MCF
FDA UDI
Class IActive
Comfort Cushion MCC001
FDA UDI
Class IActive
Gantry Guard Flex PSCTCVR2
FDA UDI
Class IIUnknown
Gantry Guard CTG01
FDA UDI
Class IIUnknown
Duraholder Y5647877
FDA UDI
Class IActive
UR-Assure 05002-00-MCF
FDA UDI
Class IActive
Duraholder Y5647882
FDA UDI
Class IActive
Duraholder Y5647881
FDA UDI
Class IActive
Gantry Guard Flex Mini PSCTCVR3
FDA UDI
Class IIUnknown
Mechanical Change In In-Vitro Micro Device K882580
FDA 510(k)
Class IActive
Securline Franseene Needle K873369
FDA 510(k)
Class IIActive
Agar Reduction In Formula For Pdc 110 & 310 Media K863164
FDA 510(k)
Class IActive
Franzen Needle Guide For Transrectal Prostate Biop K851364
FDA 510(k)
Class IIActive
Precision Culture C.a.t.s. Collect/Trans Hsv I/Ii K872507
FDA 510(k)
Class IActive
Bbl Port-A-Cul 21628 Double Swab Sulture Collectio K844369
FDA 510(k)
Class IActive
Culture Collec. Trans. Sys., Single Wet K772206
FDA 510(k)
Class IActive
Comfort Cover K161920
FDA 510(k)
Class IIActive
Securline Umbilical Cord Clamp #3505 Sterile #3515 Non-Sterile K020718
FDA 510(k)
Class IIActive
Pdc 304 Double Swab Culture Collection K791953
FDA 510(k)
Class IActive
Secureline Disposable Fetal Monitoring Straps #3860 And #3565 K994353
FDA 510(k)
Class IIActive
Bbl Port-A-Cul 21627 Single Swab Culture Collect K844370
FDA 510(k)
Class IActive
'ecurline Umbilical Cord Clamp #3500 K990737
FDA 510(k)
Class IIActive
Culture Collec. Trans. Sys., Single Dry K772208
FDA 510(k)
Class IActive
Culture Collec. Trans. Sys., Double Wet K772210
FDA 510(k)
Class IActive
Pdc 104 & Pdc 304 Style Culture Collection & Trans K844634
FDA 510(k)
Class IActive
Precision Bioport Collection & Transport System K884357
FDA 510(k)
Class IActive
Culture Collec. Trans. Sys., Double Wet K772205
FDA 510(k)
Class IActive
Securline Fine Needle Aspiration Biopsy Tray K874665
FDA 510(k)
Class IActive
Securline Surgical Skin Marker 1000 K844865
FDA 510(k)
Class IActive
Securline Surgical Skin Marker 1000 K840820
FDA 510(k)
Class IActive
Culture Collec. Trans. Sys., Double Dry K772209
FDA 510(k)
Class IActive
Franzen Needle Guide K830235
FDA 510(k)
Class IActive
Securline Umbilical Cord Clamp Clipper #3540 K994263
FDA 510(k)
Class IIActive
Pdc 104 Single Swab Culture Collection K791924
FDA 510(k)
Class IActive
Culture Collec. Trans. Sys., Single Wet K772207
FDA 510(k)
Class IActive

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Authorities

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Jul 10, 2013Z-1872-2013—terminated

PDC Healthcare initiated this recall of Non-Sterile Viscot Part Number 1437-100 Surgical Skin Markers, becuase they were inadvertently mislabeled as PN STER-VIS Sterile Skin Marker Pen with Labels and Flex Ruter.