Covidien Lp, Formerly Registered AS United States
North Haven, CT, US
Covidien Lp, Formerly Registered AS United States appears in FDA device records in North Haven, CT. FDA records list 7 510(k) clearances between and , 5 PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 7
- PMA records
- 5
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Covidien Lp, Formerly Registered AS United States between 2008 and 2009. The busiest year on record is 2009, with 4. The most recent is 2009, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2008 | 3 |
| 2009 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K091869 | SILS CLINCHER, SILS DISSECTOR, SILS GRASPER, SILS L-HOOK, SILS SHEARS | GCJ | Substantially Equivalent | |
| K091900 | ABSORBATACK 5MM SINGLE USE ABSORBABLE FIXATION DEVICE | GDW | Substantially Equivalent | |
| K083519 | AUTOSUTURE ENDO GIA STAPLERS WITH ENDO GIA SINGLE USE LOADING UNITS | GDW | Substantially Equivalent | |
| K090419 | SILS STITCH ENDOSCOPIC SUTURING DEVICE | OCW | Substantially Equivalent | |
| K082619 | SILS PORT, MODELS SILSPT5, SILSPT12 | GCJ | Substantially Equivalent | |
| K082659 | MODIFIED ENDO STICH | OCW | Substantially Equivalent | |
| K081169 | AUTOSUTURE VERSAPORT PLUS BLADLESS TROCAR; BLADELESS TROCAR | GCJ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain