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FDA 510(k)

WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX

K-Number: K920557 · 1992-03-20

ApplicantWilde-USA, Inc.
Decision Date1992-03-20
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX is the device name listed in this FDA 510(k) record. The listed applicant is Wilde-USA, Inc.. It received FDA 510(k) clearance on 1992-03-20 under 510(k) number K920557. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX?

WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX is a medical device that received FDA 510(k) clearance on 1992-03-20. The listed applicant is Wilde-USA, Inc.. The 510(k) number is K920557.

When did WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX receive FDA 510(k) clearance?

WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX received FDA 510(k) clearance on 1992-03-20, under 510(k) number K920557.

Who is the listed applicant for WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX?

The FDA 510(k) record lists Wilde-USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX?

The FDA product code for WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX is EBI.

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Other records listing Wilde-USA, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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