510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K042580Substantially Equivalent

Tidi Brand Sterilization Wrap

Banta Healthcare Group, Ltd., Clearwater FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K042580 is the FDA 510(k) clearance record for TIDI BRAND STERILIZATION WRAP, a class II device, cleared for Banta Healthcare Group, Ltd. on under FDA product code FRG (Wrap, Sterilization). FDA records list 2 510(k) clearances for Banta Healthcare Group, Ltd., from to . As of , FDA records show no recalls naming K042580.

Clearance record

Decision date
Received
(56 days to decision)
Product code
FRG Wrap, Sterilization
Regulation
21 CFR 880.6850
Device class
Class II
Review panel
General Hospital
Applicant
Banta Healthcare Group, Ltd. 2454 Mcmullen Booth Rd., Clearwater FL
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code FRG

Trailing 12 months
5 clearances under product code FRG in the twelve months to October 2026, May 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FRG, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20262
June 20260
July 20261
August 20260
September 20260
October 20260