Home › Device types › KDC
Instrument, Surgical, Disposable
FDA product code KDC · Class 1 · General, Plastic Surgery
1,320
Registered devices
866
Adverse events
38
Recalls
67
510(k) clearances
Devices with this code
Integra — ProvisionSterion® Vessel Loop — ASPEN SURGICAL PRODUCTS, INC.MSI Precision Specialty Instruments — Med Saver, Inc.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Sterion®Suture Aid Booties — ASPEN SURGICAL PRODUCTS, INC.Centurion — CENTURION MEDICAL PRODUCTS CORPORATIONCenturion — CENTURION MEDICAL PRODUCTS CORPORATIONCenturion — CENTURION MEDICAL PRODUCTS CORPORATIONIntegra — ProvisionKey Surgical Vascular Loops — KEY SURGICAL, INC.DeRoyal — DEROYAL INDUSTRIES, INC.CARDINAL HEALTH — Cardinal Health 200, LLCMonoject — Cardinal Health 200, LLCMSI Precision Specialty Instruments — Med Saver, Inc.Centurion — CENTURION MEDICAL PRODUCTS CORPORATIONBioseal Inc. — BIOSEALMagnum Medical — MAGNUM MEDICAL, INC.Richard-Allan® Vessel Loop — ASPEN SURGICAL PRODUCTS, INC.Integra — ProvisionTeleflex — ProvisionSBH — SBH SurgicalDeRoyal — DEROYAL INDUSTRIES, INC.Dermapac, Inc. — Dermapac 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 |
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