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Access Scientific, Inc.

Last updated May 23, 2026

Information

Country: US
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DUNS Number: —

Catalogue (53)

Page 1 of 2

Device	Model / Reference	Registries	Class	Status
Cvc Wand	7Fr X 6cm	FDA UDI	Class II	Active
Powerwand	ED Quick Kit 3Fr x 6cm (Custom)	FDA UDI	Class II	Active
Picc Wand	5Fr	FDA UDI	Class II	Active
Powerwand™ Xl	3Fr x 6cm	FDA UDI	Class II	Active
Powerwand	Pediatric Kit 3Fr X 6cm	FDA UDI	Class II	Active
Powerwand	Max Barrier Kit 5Fr X 8cm	FDA UDI	Class II	Active
Powerwand™ Xl	Alt Site Kit 5Fr X 8cm	FDA UDI	Class II	Active
Powerwand	Max Barrier Kit 4Fr X 8cm	FDA UDI	Class II	Active
Powerwand	ED 3Fr x 6cm (Custom)	FDA UDI	Class II	Active
Powerwand™ Xl	Alternate Site Kit 4Fr x 10cm	FDA UDI	Class II	Active
Powerwand	Quick Kit 4Fr X 8cm	FDA UDI	Class II	Active
Picc Wand	6Fr	FDA UDI	Class II	Active
Picc Wand	Max Barrier Kit 4Fr	FDA UDI	Class II	Active
Cvc Wand Xl	Max Barrier Kit	FDA UDI	Class II	Active
Cvc Wand Xl	7Fr X 6cm	FDA UDI	Class II	Active
Powerwand™ Xl	Basic Kit 4Fr X 10cm	FDA UDI	Class II	Active
Cvc Wand	Max Barrier Kit	FDA UDI	Class II	Active
Powerwand	W/Statlock	FDA UDI	Class I	Active
Powerwand	Quick Kit 3Fr X 6cm	FDA UDI	Class II	Active
Powerwand	Quick Kit 5Fr X 8cm	FDA UDI	Class II	Active
Powerwand	Quick Kit 4Fr X 10cm	FDA UDI	Class II	Active
Picc Wand	4Fr	FDA UDI	Class II	Active
Powerwand	Deluxe Dressing Change kit w/ Zpad	FDA UDI	Class I	Active
Arterial Wand	3Fr x 5cm	FDA UDI	Class II	Active
Cvc Wand	Max Barrier Kit	FDA UDI	Class II	Active
Cvc Wand	7Fr	FDA UDI	Class II	Active
Powerwand™ Xl	Basic Kit 4Fr X 8cm	FDA UDI	Class II	Active
Picc Wand	Max Barrier Kit 6Fr	FDA UDI	Class II	Active
Powerwand	3 Fr X 6 cm	FDA UDI	Class II	Active
Powerwand™ Xl	Maximum Barrier Kit 4Fr x 10cm	FDA UDI	Class II	Active
Powerwand	Max Barrier Kit 4Fr X 10cm	FDA UDI	Class II	Active
Powerwand	Dressing Change Kit with Zpad	FDA UDI	Class I	Active
Powerwand™ Xl	Alt Site Kit 4Fr X 8cm	FDA UDI	Class II	Active
Picc Wand	Max Barrier Kit 5Fr	FDA UDI	Class II	Active
Powerwand	Dressing Change Kit with StatLock	FDA UDI	Class I	Active
Powerwand™ Xl	Alt Site Kit 5Fr X 10cm	FDA UDI	Class II	Active
Powerwand Xl	Pediatric Kit 3Fr X 6cm	FDA UDI	Class II	Active
Cvc Wand Xl	7Fr	FDA UDI	Class II	Active
Powerwand™ Xl	Max Barrier Kit 5Fr X 10cm	FDA UDI	Class II	Active
The Cvc Wand Safety Introducer With Valved Peelable Sheath	K131148	FDA 510(k)	Class II	Active
The Picc Wand (r) Peelable Safety Introducer	K111138	FDA 510(k)	Class II	Active
The Picc Wand Peelable Safety Introducer	K093022	FDA 510(k)	Class II	Active
The Powerwand Safety Introducer With And Extended Dwell	K121748	FDA 510(k)	Class II	Active
Picc Wand Peelable Safety Introducer	K101150	FDA 510(k)	Class II	Active
The Wand Microaccess Safety Introducer	K090372	FDA 510(k)	Class II	Active
the POWERWAND Safety Introducer with an Extended Dwell Catheter, 3Fr. Model	K162322	FDA 510(k)	Class II	Active
The Wand Microaccess Safety Introducer, Models 90001, 90002, 90005, 90006	K081697	FDA 510(k)	Class II	Active
The ARTERIAL WAND Safety Introducer with Arterial Catheter made of ChronoFlex C with BioGUARD Technology	K181563	FDA 510(k)	Class II	Active
The Powerwand Safety Introducer With An Extended Dwell Catheter	K131300	FDA 510(k)	Class II	Active
The Powerwand (r) Safety Introducer With An Extended Dwell Catheter	K111417	FDA 510(k)	Class II	Active

Related Companies

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FDA Recalls (14)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Jun 15, 2020	Z-2550-2020	—	terminated	Convenience kit mislabeled with the incorrect catheter effective length on the device label and the packaging label. Use may lead to a delay or interruption of treatment and user dissatisfaction or annoyance.
Apr 23, 2020	Z-1974-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Apr 23, 2020	Z-1979-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Apr 23, 2020	Z-1976-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Apr 23, 2020	Z-1981-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Apr 23, 2020	Z-1973-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Apr 23, 2020	Z-1978-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Apr 23, 2020	Z-1983-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Apr 23, 2020	Z-1977-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Apr 23, 2020	Z-1982-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Apr 23, 2020	Z-1980-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Apr 23, 2020	Z-1972-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Apr 23, 2020	Z-1975-2020	—	terminated	Saline Flush Syringe compromised sterility due to holes in the packaging.
Aug 16, 2013	Z-2254-2013	—	terminated	Access Scientific is recalling the POWERWAND Saftey Introducer with Extended Dwell Catheter because it is mislabeled.