510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K051950Substantially Equivalent

Inscope Multi-Clip Applier, Models In22321, In23321

Ethicon Endo-Surgery Inc, Cincinnati OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K051950 is the FDA 510(k) clearance record for INSCOPE MULTI-CLIP APPLIER, MODELS IN22321, IN23321, a class II device, cleared for Ethicon Endo-Surgery, Inc. on under FDA product code MND (Ligator, Esophageal). FDA records list 185 510(k) clearances for Ethicon Endo-Surgery, Inc., from to . As of , FDA records show no recalls naming K051950.

Clearance record

Decision date
Received
(81 days to decision)
Product code
MND Ligator, Esophageal
Regulation
21 CFR 876.4400
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Ethicon Endo-Surgery, Inc. 4545 Creek Rd., Cincinnati OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MND

Trailing 12 months

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

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