DeviceClearance

Product code NLQ— Unknown

Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector

Classification name
Single-Use Reprocessed Ultrasonic Surgical Instruments
Device class
Unclassified
Advisory panel
Unknown
Total cleared
27
First cleared
Most recent

FDA classification definition

“Single-use reprocessed versions of the ultrasonic devices used in surgical procedures either for fragmentation, emulsification and aspiration of soft tissue and hard tissue or for ligation of vessels (under product code “LFL”). Reprocessing validation data for this device type must be included in a 510(k) submission.. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).”

— U.S. Food and Drug Administration, device classification record for product code NLQ, via openFDA

Market context for product code NLQ

FDA has cleared 27 devices under product code NLQ between 2001 and 2025, filed by 11 applicant companies. No FDA device recalls reference this product code.

Clearances per year

last 15 years

Top applicants under product code NLQ

Recent clearances under product code NLQ

Data sourced from openFDA. This site is unofficial and independent of the FDA.