510(k) clearances

Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)

Stryker Instruments · General, Plastic Surgery

K261959Substantially EquivalentSpecialGEI
Open FDA's page for this record
Third party flag
N
City
Portage
Advisory committee description
General, Plastic Surgery
Address 1
1941 Stryker Way
Statement or summary
Summary
Product code
GEI
Zip code
49002
Applicant
Stryker Instruments
Decision date
2026-09-17
Decision code
SESE
Country code
US
Advisory committee
SU
Contact
Jessica Brophy
K number
K261959
State
MI
Date received
2026-06-11
Review advisory committee
SU
Postal code
49002
Decision description
Substantially Equivalent
Clearance type
Special
Device name

Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)

Harmonized identifiers (openFDA)
Device name
Electrosurgical, Cutting & Coagulation & Accessories
Medical specialty description
General, Plastic Surgery
Regulation number
878.4400
Device class
2
Registration number
2184009, 1221934, 3013176080, 9680952, 3003678543, 3009380063, 3009881188, 2245590, 2431166, 3006849754, 2029275, 3004111573, 2133786, 3009882464, 3013283620, 3012447612, 3007710878, 2648623, 3004122598, 3015612252, 3010280625, 1929938, 3012497308, 3009762450, 3010288205, 3012322232, 3018242561, 1836161, 2020394, 1222993, 3006891627, 9610614, 2955842, 3011879048, 3013466775, 2032098, 3004636440, 3012790575, 9614969, 3007583504 +832 more
FEI number
1221934, 3013176080, 3003678543, 3009380063, 3009881188, 2245590, 3006849754, 3004111573, 3009882464, 3013283620, 3002808445, 3012447612, 3007710878, 2648623, 3004122598, 3015612252, 3010280625, 1929938, 3012497308, 3009762450, 3010288205, 3012322232, 3018242561, 2020394, 3006891627, 1000518731, 3011879048, 1000112877, 3013466775, 1000160458, 3002900199, 1000122656, 3003186357, 3004636440, 3012790575, 3007583504, 3040335671, 3009420598, 3010164891, 3003448211 +832 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.