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FDA 510(k)

COMPATIT R

K-Number: K913582 · 1993-06-24

ApplicantWilde-USA, Inc.
Decision Date1993-06-24
Product CodeELM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COMPATIT R 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 1993-06-24 under 510(k) number K913582. The device is classified under product code ELM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPATIT R?

COMPATIT R is a medical device that received FDA 510(k) clearance on 1993-06-24. The listed applicant is Wilde-USA, Inc.. The 510(k) number is K913582.

When did COMPATIT R receive FDA 510(k) clearance?

COMPATIT R received FDA 510(k) clearance on 1993-06-24, under 510(k) number K913582.

Who is the listed applicant for COMPATIT R?

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 COMPATIT R?

The FDA product code for COMPATIT R is ELM.

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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.

K915653KERAMAILK913581WILDE ADHESIVE BONDING SYSTEMK923472COMPACOLORK920649COMPASEPK915250WIL-PDS & WIL-PDI CASTING ALLOYSK913089WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS

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Related Devices (Code: ELM)

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.

K122955DENTAVIT, MONARCH, ACROTONE, SENATOR, DENTORIUMWright Health Group , Ltd.K122925NEW STETIC ARTIFICIAL TEETHNew SteticK122852PHYSIOSTAR NFCCandulor USA, Inc.K121749VERACIAShofu Dental CorporationK120404MERZ DENTAL GMBH ARTEGRAL HD PREFORMED PLASTIC DENTURE TEETHMerz Dental GmbHK120736SR PHONARES IIIvoclar Vivadent, AG

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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