Scican , Ltd.
Scican , Ltd. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2022, with 2 FDA device recalls on record.
Top product codes for Scican , Ltd.
FDA recalls by Scican , Ltd.
- Z-2285-2023 — STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use by a health care provider to sterilize medical products by means of pressurized steam. Model: G4 621103
- Z-2286-2023 — STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use by a health care provider to sterilize medical products by means of pressurized steam. Model: G4 622303
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Scican , Ltd.
- K214057 — STATIM 6000B Vacuum Autoclave
- K210326 — Bravo G4 Chamber Autoclave
- K192910 — STATClave G4 Chamber Autoclave
- K190062 — STATCLAVE G4 Chamber Autoclave
- K172292 — SALUS - Hygiene Instrument Reprocessing Container
- K112872 — STATIM 2000 G4 CASSETTE
- K090937 — E-STATIS 40 SYSTEM
- K090265 — BRAVO AUTOCLAVE, MODELS 17, 17V AND 21V
- K073319 — STATMATIC 31 HANDPIECE MAINTENANCE UNIT
- K072466 — STATIM 7000 (WITHOUT USB PORT), MODEL 01-702100, STATIM 7000 (WITH USB PORT), MODEL 01-702101
- K071891 — STATIS DENTAL HANDPIECES
Data sourced from openFDA. This site is unofficial and independent of the FDA.