Skip to content

Danville Materials, LLC

Also registered as Danville Materials, Inc., Daville Materials, LLC

United StatesFDA applicant, unverified

Danville Materials, LLC is a medical device manufacturer, with 260 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I) and 1 FDA recall as of 12 Nov 2026.

Devices
260
FDA recalls
1

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 243
  • EUDAMED 106
  • FDA 510(k) 17

A device listed in two registries counts in both.

Device classes
  • FDA Class II 239
  • FDA Class I 21
Identifiers
  • DUNS 601302743

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

Catalogue260

Newest first, rows 1-50 of 260

Search and filter all 260 devices
Skip device list
  • Startflow 89397

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • First Quarter 90901

    Listed Registry: GUDID Class:II
  • Accolade Pv 91237

    Listed Registry: GUDID Class:II
  • Pontic 90138

    Listed Registry: GUDID Class:II
  • Sky Select KY9032

    Listed Registry: GUDID Class:II
  • Start Vps 93718

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Accolade Pv 90559

    Listed Registry: GUDID Class:II
  • Aria 89356

    Listed Registry: GUDID Class:II
  • Microetcher 201935-00

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • First Half 90650

    Listed Registry: GUDID Class:II
  • Sky Select KY9030

    Listed Registry: GUDID Class:II
  • Prelude 94072

    Listed Registry: GUDID Class:II
  • Rock Core 93831

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Accolade 90556

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Microetcher 201936-00

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • First Half 91122

    Listed Registry: GUDID Class:II
  • Startflow 89035

    Listed Registry: GUDID Class:II
  • Prelude 94037

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Microetcher 22000-03

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Start Vps 80061-01

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Fusion FTXA3

    Listed Registry: GUDID Class:II
  • Startflow 90750

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Startflow 85056

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Fusion FHA1

    Listed Registry: GUDID Class:II
  • Contact Matrix 91974

    Listed Registry: GUDID Class:I
  • Rock Core 90838

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Viax 94941

    Listed Registry: GUDID Class:II
  • First Half 91244

    Listed Registry: GUDID Class:II
  • First Half 91124

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Accolade Pv 91235

    Listed Registry: GUDID Class:II
  • Sky Select KY9035

    Listed Registry: GUDID Class:II
  • Startflow 85059

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Turbo Temp 2 90156

    Listed Registry: GUDID Class:II
  • Prelude 91657

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Contact Matrix 94272

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • First Quarter 90729

    Listed Registry: GUDID Class:II
  • Turbo Temp 2 90158

    Listed Registry: GUDID Class:II
  • Start Vps 93554

    Listed Registry: GUDID Class:II
  • Accolade 90558

    Listed Registry: GUDID Class:II
  • Accolade Sro 91387

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Start Vps 80013-01

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Start Vps 93553

    Listed Registry: GUDID Class:II
  • First Half 90469

    Listed Registry: GUDID Class:II
  • Contact Matrix 90071

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • Sky Select KY9034

    Listed Registry: GUDID Class:II
  • Accolade Sro 91416

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Startflow 89037

    Listed Registry: GUDID Class:II
  • Turbo Temp 2 92964

    Listed Registry: GUDID Class:II
  • Accolade Sro 91388

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • First Quarter 89272

    Listed Registry: GUDID Class:II

Rows 1-50 of 260

Showing 1-50 of 260

Company details

DUNS number
601302743
Phone
+1(760)743-7744

FDA recalls1

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

  • 2016

    • 24 Jun 2016 Z-2530-2016 Class II Terminated The Perioscopy Sheaths are currently provided with a label that indicates the Sheath has a 3 year shelf-life/expiry date. Danville Materials has become aware that validation data are not available to support the 3-year shelf-life/expiration dating claim. Distribution: US and New Zealand, Australia, Canada, Japan, Israel, United Kingdom, Italy, Mexico. Submission number: K982480

Frequently asked questions

How many devices does DANVILLE MATERIALS, LLC have in the registry?

The registry currently lists 260 devices for DANVILLE MATERIALS, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list DANVILLE MATERIALS, LLC's devices?

Among its 50 most recently registered devices, DANVILLE MATERIALS, LLC has devices listed in EUDAMED (21 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do DANVILLE MATERIALS, LLC's devices fall under?

Among its 50 most recently registered devices, the classes recorded for DANVILLE MATERIALS, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for DANVILLE MATERIALS, LLC?

FDA recall records list 1 recall initiated by DANVILLE MATERIALS, LLC, the most recent initiated on 24 Jun 2016. 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 DANVILLE MATERIALS, LLC in the registry?

The most recently registered devices listed for DANVILLE MATERIALS, LLC include STARTFLOW 89397, FIRST QUARTER 90901, ACCOLADE PV 91237 and PONTIC 90138.

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