Home › Device types › KDC
Instrument, Surgical, Disposable
FDA product code KDC · Class 1 · General, Plastic Surgery
1,354
Registered devices
896
Adverse events
38
Recalls
67
510(k) clearances
Devices with this code
NA — KEY SURGICAL, INC.SCANLAN® Ultimate® A/V Punch — SCANLAN INTERNATIONAL INCMSI Precision Specialty Instruments — Med Saver, Inc.DeRoyal — DEROYAL INDUSTRIES, INC.Sterion® Vessel Loop — ASPEN SURGICAL PRODUCTS, INC.DEJA VU — Cardinal Health 200, LLCDeRoyal — DEROYAL INDUSTRIES, INC.SCANLAN® A/V Punch — SCANLAN INTERNATIONAL INCCenturion — CENTURION MEDICAL PRODUCTS CORPORATIONAllen Medical — ProvisionDermapac, Inc. — Dermapac Inc.HNM MEDICAL — HNM STAINLESS, LLC.MSI Precision Specialty Instruments — Med Saver, Inc.MSI Precision Specialty Instruments — Med Saver, Inc.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.N/A — Summit Medical, Inc.Bioseal Inc. — BIOSEALConmed/Linvatec — ProvisionScanlan® SUTURE BOOT™ Instrument Jaw Covers — SCANLAN INTERNATIONAL INCSuture Clamp Tags, Sterile — Batrik Medical Manufacturing IncConmed/Linvatec — ProvisionDeRoyal — DEROYAL INDUSTRIES, INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Bioseal Inc. — BIOSEAL
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-04-09 | MEDLINE INDUSTRIES, LP - Northfield | Three is the potential for the retractors to puncture through the sterile packaging. |
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
| 2022-10-12 | Medical Action Industries, Inc. 306 | Scissors contained debris. |
| 2021-05-11 | Medical Action Industries, Inc. 306 | There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits |
| 2021-05-11 | Medical Action Industries, Inc. 306 | There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits |
| 2016-08-01 | Ethicon, Inc. | ETHICON MERSILENE" Tape (also referred to as MERSILENETM Polyester Fiber Strip or MERSILENETM Fiber Ligature) products are being recalled since a group of MERSI |
| 2011-03-28 | Hospira Inc. | There is a potential for the air filter at the distal end of the set to become detached. This could result in the contamination of the sterile fluid path insid |
| 2011-03-28 | Hospira Inc. | There is a potential for the air filter at the distal end of the set to become detached. This could result in the contamination of the sterile fluid path insid |
| 2011-03-28 | Hospira Inc. | There is a potential for the air filter at the distal end of the set to become detached. This could result in the contamination of the sterile fluid path insid |
| 2011-03-28 | Hospira Inc. | There is a potential for the air filter at the distal end of the set to become detached. This could result in the contamination of the sterile fluid path insid |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.