510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K901321Substantially Equivalent

Sharp-Safe, Biodegradeable,disp., Needle Disp. Box

Sharp Safe, Inc., Southfield MI / Traditional, Substantially Equivalent

K901321 is the FDA 510(k) clearance record for SHARP-SAFE, BIODEGRADEABLE,DISP., NEEDLE DISP. BOX, cleared for Sharp Safe, Inc. on under FDA product code LDQ. FDA records list one 510(k) clearance for Sharp Safe, Inc. As of , FDA records show no recalls naming K901321.

Clearance record

Decision date
Received
(51 days to decision)
Product code
LDQ
Review panel
General Hospital
Applicant
Sharp Safe, Inc. 15777 W. Ten Mile, Southfield MI
Third party review
No

Clearances, product code LDQ

Trailing 12 months

FDA records hold no clearances under product code LDQ in the trailing twelve months.

FDA records show no clearances under product code LDQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LDQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260