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Wilde-USA, Inc.

Naperville, IL, US

Wilde-USA, Inc. appears in FDA device records in Naperville, IL. FDA records list 16 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
16
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 16 510(k) clearances for Wilde-USA, Inc. between 1991 and 1993. The busiest year on record is 1992, with 8. The most recent is 1993, with 3.

Clearances by year, as a table
510(k) clearance decisions for Wilde-USA, Inc., by decision year
YearClearances
19915
19928
19933
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K913582COMPATIT RELMSubstantially Equivalent
K915653KERAMAILEIHSubstantially Equivalent
K913581WILDE ADHESIVE BONDING SYSTEMKLESubstantially Equivalent
K923472COMPACOLOREBFSubstantially Equivalent
K920649COMPASEPFMCSubstantially Equivalent
K915250WIL-PDS & WIL-PDI CASTING ALLOYSEJHSubstantially Equivalent
K913089WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINSEBFSubstantially Equivalent
K912990CONVERBASEEBISubstantially Equivalent
K920557WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUXEBISubstantially Equivalent
K915654KERALLOY-D CAPSEJJSubstantially Equivalent
K912993WILDE DENTURE RESINSEBISubstantially Equivalent
K912994COMPALUX STROBOSCOPIC LIGHT POLYMERIZATION DEVICEEBZSubstantially Equivalent
K912991WILDE AUXILIARIESEBISubstantially Equivalent
K913583CONVERSIL FL AND CONVERSIL PELWSubstantially Equivalent
K912992KERALLOY NON-GAMMA 2 AMALGAMEJJSubstantially Equivalent
K912989PLANUSTAR AND DENS NOBILIS DENTURE TEETHEMISubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain