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T-STRIP
PRECISION MEDICAL DEVICES, LLC · Model TS-001 · UDI-DI 00869193000002
1
510(k) clearances
4
Adverse events
9
Recalls
38
Facilities
Description
The T-Strip is a 2.0 X 7.5 cm porous mesh wound closure strip that allows quick, and easy approximation of the edges of traumatic wounds; while reducing wound tension. The transparent T-Strip allows ideal wound approximation; simply apply to one side of the wound, then gently pull across the wound while aligning the edges. Adhere the remaining adhesive mesh to the other side of the wound, then apply a topical skin adhesive (skin glue) directly on and through the T-strip, sealing the wound.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.