Sherlock
K-Number: K220482 · 2022-06-21
ApplicantOpen Implants, LLC
Decision Date2022-06-21
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Sherlock is a medical device manufactured by Open Implants, LLC. It received FDA 510(k) clearance on 2022-06-21 under approval number K220482. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Sherlock?
Sherlock is a medical device that received FDA 510(k) clearance on 2022-06-21. It is manufactured by Open Implants, LLC. The 510(k) number is K220482.
When was Sherlock approved by the FDA?
Sherlock received FDA 510(k) clearance on 2022-06-21, under approval number K220482.
What company makes Sherlock?
Sherlock is manufactured by Open Implants, LLC.
What is the FDA product code for Sherlock?
The FDA product code for Sherlock is NHA.
Other Devices by Open Implants, LLC
Related Devices (Code: NHA)
K161713Dentium CAD/CAM AbutmentsDentium Co., Ltd.
K160798IPS e.max® Press Abutment Solutions for Viteo Base TiIvoclar Vivadent, AG
K162004PREMIUM Implant Systems SHELTA Implant SystemsSweden & Martina S.P.A.
K153015Transfer & Angled AbutmentOsstem Implant Co., Ltd.
K161435Temporary Snap AbutmentNobel Biocare AB
K160786RODO Abutment SystemRodo Medical, 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.