510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K803067Substantially Equivalent

Surg-Flex 10 Light

Medical Products Development, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K803067 is the FDA 510(k) clearance record for SURG-FLEX 10 LIGHT, a class II device, cleared for Medical Products Development, Inc. on under FDA product code FSQ (Light, Surgical, Instrument). FDA records list 13 510(k) clearances for Medical Products Development, Inc., from to . As of , FDA records show no recalls naming K803067.

Clearance record

Decision date
Received
(84 days to decision)
Product code
FSQ Light, Surgical, Instrument
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Medical Products Development, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FSQ

Trailing 12 months

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

FDA records show no clearances under product code FSQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FSQ, 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