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FDA 510(k)

OMNI-FIL

K-Number: K863876 · 1986-11-26

ApplicantInpromas
Decision Date1986-11-26
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OMNI-FIL is the device name listed in this FDA 510(k) record. The listed applicant is Inpromas. It received FDA 510(k) clearance on 1986-11-26 under 510(k) number K863876. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMNI-FIL?

OMNI-FIL is a medical device that received FDA 510(k) clearance on 1986-11-26. The listed applicant is Inpromas. The 510(k) number is K863876.

When did OMNI-FIL receive FDA 510(k) clearance?

OMNI-FIL received FDA 510(k) clearance on 1986-11-26, under 510(k) number K863876.

Who is the listed applicant for OMNI-FIL?

The FDA 510(k) record lists Inpromas as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OMNI-FIL?

The FDA product code for OMNI-FIL is EBF.

Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, Inc.

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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