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Precision Dynamics Corporation

Also registered as Precision Dynamics Corp.

United Statesfrom the FDA registration address FDA establishment FEI 2020282

Precision Dynamics Corporation is a medical device manufacturer, with 44 devices listed in FDA 510(k) and FDA GUDID (FDA Class I and II) and 1 FDA recall as of 14 Nov 2026.

Devices
44
Registrations
FDA
FDA recalls
1

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • FDA 510(k) 26
  • FDA GUDID 18

A device listed in two registries counts in both.

Device classes
  • FDA Class I 31
  • FDA Class II 13
Identifiers
  • FDA FEI 2020282

Catalogue44

Newest first, rows 1-44 of 44

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Rows 1-44 of 44

Company details

FDA FEI number
2020282
Address
25124 Springfield Ct Ste 200, Valencia, CA, 91355

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

  • 2013

    • 10 Jul 2013 Z-1872-2013 Class II 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. Distribution: US Distribution including the states of SC, TX, TN, WA, OK.

Frequently asked questions

How many devices does PRECISION DYNAMICS CORPORATION have in the registry?

The registry currently lists 44 devices for PRECISION DYNAMICS CORPORATION. Devices recorded under merged duplicate company entries are counted once.

Which registries list PRECISION DYNAMICS CORPORATION's devices?

Among its 44 most recently registered devices, PRECISION DYNAMICS CORPORATION has devices listed in FDA 510(k) (26 devices) and FDA GUDID (18 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do PRECISION DYNAMICS CORPORATION's devices fall under?

Among its 44 most recently registered devices, the classes recorded for PRECISION DYNAMICS CORPORATION's devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for PRECISION DYNAMICS CORPORATION?

FDA recall records list 1 recall initiated by PRECISION DYNAMICS CORPORATION, the most recent initiated on 10 Jul 2013. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from PRECISION DYNAMICS CORPORATION in the registry?

The most recently registered devices listed for PRECISION DYNAMICS CORPORATION include Duraholder Y5647879, Comfort Cushion MCC002, Gantry Guard Flex Mini CTG03 and Gantry Guard SCTG01.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company.