510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K845023Substantially Equivalent

Storz Plastic Surgery & Examination Lounge 7000

Storz Instrument Co., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K845023 is the FDA 510(k) clearance record for STORZ PLASTIC SURGERY & EXAMINATION LOUNGE 7000, a class I device, cleared for Storz Instrument Co. on under FDA product code LGX (Table, Examination, Medical, Powered). FDA records list 101 510(k) clearances for Storz Instrument Co., from to . As of , FDA records show no recalls naming K845023.

Clearance record

Decision date
Received
(32 days to decision)
Product code
LGX Table, Examination, Medical, Powered
Regulation
21 CFR 878.4960
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Storz Instrument Co. 3365 Tree Ct. Industrial Blvd., St. Louis MO
Third party review
No

Clearances, product code LGX

Trailing 12 months

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

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