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FDA 510(k)

IMPAC TORQUE WRENCH

K-Number: K940998 · 1994-11-21

ApplicantVident
Decision Date1994-11-21
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPAC TORQUE WRENCH is the device name listed in this FDA 510(k) record. The listed applicant is Vident. It received FDA 510(k) clearance on 1994-11-21 under 510(k) number K940998. 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 IMPAC TORQUE WRENCH?

IMPAC TORQUE WRENCH is a medical device that received FDA 510(k) clearance on 1994-11-21. The listed applicant is Vident. The 510(k) number is K940998.

When did IMPAC TORQUE WRENCH receive FDA 510(k) clearance?

IMPAC TORQUE WRENCH received FDA 510(k) clearance on 1994-11-21, under 510(k) number K940998.

Who is the listed applicant for IMPAC TORQUE WRENCH?

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

What is the FDA product code for IMPAC TORQUE WRENCH?

The FDA product code for IMPAC TORQUE WRENCH is DZE.

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Other records listing Vident 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.

K063768TITANIUM SCALLOPED ABUTMENTK060441VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9, MODEL NX98K052710VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9,K052130VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40K050362VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)K022996VITA IN-CERAM YZ CUBES FOR CEREC

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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

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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