510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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DEN080011Unknown

Snap Wound Care Device

Spiracur, Inc., Philadelphia PA / Post-NSE, Unknown
FDA source (opens on fda.gov)

DEN080011 is the FDA 510(k) clearance record for SNAP WOUND CARE DEVICE, a class II device, cleared for Spiracur, Inc. on under FDA product code OKO (Negative Pressure Wound Therapy Non-Powered Suction Apparatus). FDA's definition for product code OKO reads: "A non-powered suction apparatus indicated for negative pressure wound therapy (npwt) that is intended for wound management via application of continual or intermittent negative pressure to the wound for removal of fluids, including wound...". FDA records list 9 510(k) clearances for Spiracur, Inc., from to . As of , FDA records show no recalls naming DEN080011.

Clearance record

Decision date
Received
(277 days to decision)
Product code
OKO Negative Pressure Wound Therapy Non-Powered Suction Apparatus
Regulation
21 CFR 878.4683
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Spiracur, Inc. 1835 Market St., Suite 2820, Philadelphia PA
Third party review
No

Clearances, product code OKO

Trailing 12 months
1 clearance under product code OKO in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code OKO, 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 20261
October 20260