Single Use Instrument Tray
General, Plastic Surgery · 21 CFR 878.4800
This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance
Recent MDR events
6 adverse event reports on file
- ONESTEPMar 9, 2026InjuryMerit Medical Systems, Inc.1721504-2026-00905
- LACERATION TRAYSep 17, 2025MalfunctionCardinal Health 200, LlcMW5176207
- PRESOURCE LACERATION TRAYSep 15, 2025MalfunctionCardinal Health 200, LlcMW5176071
- SINGLE USE INSTRUMENT TRAYNov 30, 2022Malfunction15885709
- SPECTRANETICS BRIDGE BALLOON PREP KITMar 1, 2018InjuryMerit Medical Systems Inc1721504-2018-00022
- GYN DISPOSABLES TENACULUM 356T (COMPONENT OF GYN DISPOSABLES 935K IUD INSERTIONSep 21, 2012MalfunctionGyn DisposablesMW5027079
Event type breakdown
Recalls
38 recall events for this product code
- Merit Medical Systems, Inc.TerminatedNov 19, 2016
Fluid Management Set. Catalog Number K08-MP5159A
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
Z-0631-2017 · View FDA record ↗ - Merit Medical Systems, Inc.TerminatedNov 19, 2016
Manifold Kit. Catalog Number K09-11867AP
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
Z-0632-2017 · View FDA record ↗ - Merit Medical Systems, Inc.TerminatedNov 19, 2016
Waste Management Kit. Catalog Number K10-04381AP
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
Z-0633-2017 · View FDA record ↗ - Merit Medical Systems, Inc.TerminatedNov 19, 2016
Pressure Monitoring Kit (MeriTrans"). Catalog Number K11-00232G
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
Z-0634-2017 · View FDA record ↗ - Merit Medical Systems, Inc.TerminatedNov 19, 2016
Procedure Kit. Catalog Numbers K12-04830B and K12-YP030A
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
Z-0635-2017 · View FDA record ↗ - Medical Device Technologies, Inc.TerminatedNov 18, 2011
Angiotech***T-Lok Ecomony Bone Marrow Tray***1 - #11 Mini Scalpel; 1 - 21ga x 1-1/2" Needle; 1 - 25ga x 5/8" Needle; 1 - 19ga x 1-1/2" Filter Needle; 1 - 5cc S
Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
Z-0216-2012 · View FDA record ↗ - Medical Device Technologies, Inc.TerminatedNov 18, 2011
Angiotech***T-Lok Ecomony Bone Marrow Tray***1 - #11 Mini Scalpel; 1 - 21ga x 1-1/2" Needle; 1 - 25ga x 5/8" Needle; 1 - 19ga x 1-1/2" Filter Needle; 1 - 5cc S
Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
Z-0217-2012 · View FDA record ↗ - Medical Device Technologies, Inc.TerminatedNov 18, 2011
Angiotech***T-Lok Ecomony Bone Marrow Tray***1 - #11 Mini Scalpel; 1 - 21ga x 1-1/2" Needle; 1 - 25ga x 5/8" Needle; 1 - 19ga x 1-1/2" Filter Needle; 1 - 5cc S
Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
Z-0218-2012 · View FDA record ↗ - Medical Device Technologies, Inc.TerminatedNov 18, 2011
Angiotech***T-Lok Bone Marrow Tray***1 - #11 Mini Scalpel; 1 - 21ga x 1-1/2" Needle; 1 - 25ga x 5/8" Needle; 1 - 19ga x 1-1/2" Filter Needle; 1 - 5cc Syringe L
Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
Z-0219-2012 · View FDA record ↗ - Medical Device Technologies, Inc.TerminatedNov 18, 2011
Angiotech***Bone Marrow Tray***1 - 20cc Syringe L/L; 1 - 5cc Syringe L/L; 1 - 19ga x 1-1/2" Filter Needle; 1 - 21ga x 1-1/2" Needle; 1 - 25ga x 5/8" Needle; 1 -
Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
Z-0220-2012 · View FDA record ↗
Registered firms
39 firms currently registered for this product code
Synthes (usa) Products Llc
West Chester, PA, US
Sterigenics Us Llc
Grand Prairie, TX, US
Merit Medical Systems, Inc.
South Jordan, UT, US
Midwest Sterilization Corp.
LAREDO, TX, US
Merz North America, Inc.
FRANKSVILLE, WI, US
Sterigenics U.s., Llc
Ontario, CA, US
Merit Medical Asia Company Limited
Tsim Sha Tsui, HK
Isomedix Operations Inc
El Paso, TX, US
Merit Medical Nederland Bv
Maastricht Airport Limburg, NL
Merit Medical Uk Limited
Earley Reading, GB
Merit Medical Australia Pty Ltd.
Braiside Victoria, AU
Picocyl
Golden, CO, US
Sterigenics Belgium Petit Rechain S.a.
Verviers Liege, BE
Highridge Medical, Llc
Westminster, CO, US
Cardinal Health 200, Llc
Waukegan, IL, US
Merit Maquiladora Mexico, S. De R.l. De C.v.
Tijuana Baja California, MX
Honduras Kitting, S.a.
Villanueva Cortes, HN
Terumo Bct Sterilization Services, Inc.
LAKEWOOD, CO, US
Ssc- Surgical Specialties Corporation
Chula Vista, CA, US
Synthes Gmbh
Zuchwil Solothurn, CH
Avid Medical, Inc. A Medical Action Ind. Company 305
TOANO, VA, US
Picocyl
Golden, CO, US
Medical Action Industries, Inc. 306
ARDEN, NC, US
Isomedix Operations Inc
EL PASO, TX, US
Sterigenics U.s., Llc
Salt Lake City, UT, US
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.