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FDA 510(k)

INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM

K-Number: K103194 · 2011-04-21

ApplicantIntra-Lock International, Inc.
Decision Date2011-04-21
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM is the device name listed in this FDA 510(k) record. The listed applicant is Intra-Lock International, Inc.. It received FDA 510(k) clearance on 2011-04-21 under 510(k) number K103194. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM?

INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM is a medical device that received FDA 510(k) clearance on 2011-04-21. The listed applicant is Intra-Lock International, Inc.. The 510(k) number is K103194.

When did INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM receive FDA 510(k) clearance?

INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM received FDA 510(k) clearance on 2011-04-21, under 510(k) number K103194.

Who is the listed applicant for INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM?

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

What is the FDA product code for INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM?

The FDA product code for INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM is DZE.

Related Clinical Trials

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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Other records listing Intra-Lock International, 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.

K171831Intra-Lock Bone Fixation SystemK111199INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM 3.4MM IMPLANT ANGLED ABUTMENTSK082419REOSS POWDER, REOSS PUTTY, REOSS GEL, MODELS R-1,RP-1, RG-1

Related Devices (Code: DZE)

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

Official Source

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

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