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FDA 510(k)

SECURE RELINE/PICKUP MATERIAL

K-Number: K021586 · 2002-06-14

ApplicantImtec Corp.
Decision Date2002-06-14
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SECURE RELINE/PICKUP MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Imtec Corp.. It received FDA 510(k) clearance on 2002-06-14 under 510(k) number K021586. 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 SECURE RELINE/PICKUP MATERIAL?

SECURE RELINE/PICKUP MATERIAL is a medical device that received FDA 510(k) clearance on 2002-06-14. The listed applicant is Imtec Corp.. The 510(k) number is K021586.

When did SECURE RELINE/PICKUP MATERIAL receive FDA 510(k) clearance?

SECURE RELINE/PICKUP MATERIAL received FDA 510(k) clearance on 2002-06-14, under 510(k) number K021586.

Who is the listed applicant for SECURE RELINE/PICKUP MATERIAL?

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

What is the FDA product code for SECURE RELINE/PICKUP MATERIAL?

The FDA product code for SECURE RELINE/PICKUP MATERIAL is EBI.

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Other records listing Imtec Corp. 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.

K081653MDI MII ONE-PIECE IMPLANT, 2.9MMK081347ILUMA VISIONK072660ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114K053046ILUMA ORTHOCAT/DENTALCATK043226ENDURE IMPLANT, MODELS 3508, 4308, 3520, 4320K042289MDI ORTHO

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Related Devices (Code: EBI)

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.

K261802Glidewell™ Denture Base ResinPrismatik Dentalcraft, Inc.K261626UltraPrint Flexible Denture UVGuangzhou Heygears IMC., Inc.K262681NanoCeram Resin3BFAB TEKNOLOJI A.S.K262300Denture Base Resin V2Formlabs Ohio, Inc.K261474DENTCA Tru FlexibleDentca, Inc.K260569DB 4000 High Impact Denture BaseCarbon, 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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