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MicroAire Surgical Instruments LLC

United States·US-MF-000004063

Last updated September 17, 2026

Information

Country: United States
Address: 3590 Grand Forks Boulevard, Charlottesville, United States
Website: microaire.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: —
PRRC Contact: Chad Wade
EUDAMED SRN: US-MF-000004063
FDA FEI Number: 2020601
DUNS Number: —

Catalogue (1286)

Page 9 of 26

Device	Model / Reference	Registries	Class	Status
MicroAire®	5740-010S	FDA UDI	Class II	Unknown
MicroAire®	1600-435	FDA UDI	Class II	Active
MicroAire®	200138103S	FDA UDI	Class I	Active
MicroAire®	ZS-510	FDA UDI	Class I	Active
MicroAire®	ZB-584	FDA UDI	Class I	Active
MicroAire®	PAL-404LLB	FDA UDI	Class II	Active
MicroAire®	PAL-40HLL	FDA UDI	Class II	Active
MicroAire®	8053-015	FDA UDI	Class I	Active
MicroAire®	K-09	FDA UDI	Class I	Unknown
MicroAire®	ZO-7172	FDA UDI	Class I	Active
MicroAire®	1200-012	FDA UDI	Class I	Active
MicroAire®	ZS-329	FDA UDI	Class I	Active
MicroAire®	ZO-7111	FDA UDI	Class I	Unknown
MicroAire®	1000-100	FDA UDI	Class I	Active
MicroAire®	SP-412A	FDA UDI	Class I	Unknown
MicroAire®	ZO-7651	FDA UDI	Class I	Unknown
MicroAire®	8054-020	FDA UDI	Class I	Active
MicroAire®	1601-564	FDA UDI	Class II	Active
MicroAire®	ZO-063	FDA UDI	Class I	Active
MicroAire®	K-43	FDA UDI	Class I	Unknown
MicroAire®	8054-013NS	FDA UDI	Class I	Active
MicroAire®	8053-025NS	FDA UDI	Class I	Active
MicroAire®	ASP-CBL-1020	FDA UDI	Class II	Active
MicroAire®	8054-014	FDA UDI	Class I	Active
MicroAire®	ZB-113	FDA UDI	Class I	Active
MicroAire®	1632-509TNS	FDA UDI	Class II	Active
MicroAire®	ZB-164	FDA UDI	Class I	Active
MicroAire®	7505	FDA UDI	Class I	Active
MicroAire®	1000-200	FDA UDI	Class I	Active
MicroAire®	XZS-338	FDA UDI	Class I	Unknown
MicroAire®	ZO-070	FDA UDI	Class I	Active
MicroAire®	ZS-363	FDA UDI	Class I	Active
MicroAire®	8054-017	FDA UDI	Class I	Active
MicroAire®	ZO-066	FDA UDI	Class I	Active
MicroAire®	5950	FDA UDI	Class I	Active
MicroAire®	1600-654NS	FDA UDI	Class II	Active
MicroAire®	1624-709T	FDA UDI	Class II	Active
MicroAire®	1600-662T	FDA UDI	Class II	Active
MicroAire®	1640-109NS	FDA UDI	Class II	Active
MicroAire®	1604-154NS	FDA UDI	Class II	Active
MicroAire®	6686	FDA UDI	Class I	Active
MicroAire®	6673	FDA UDI	Class I	Active
MicroAire®	1600-654TNS	FDA UDI	Class II	Active
MicroAire®	PAL-750-PN	FDA UDI	Class II	Active
MicroAire®	SP-414	FDA UDI	Class I	Unknown
MicroAire®	ZO-7226	FDA UDI	Class I	Active
MicroAire®	INF-FOOT-1	FDA UDI	Class II	Active
MicroAire®	1648-109NS	FDA UDI	Class II	Active
MicroAire®	1620-709	FDA UDI	Class II	Active
MicroAire®	5006-1000	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

MediMark Europe Sarl. FR

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (16)

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
May 7, 2025	Z-1975-2025	—	open, classified	Potential that the blade can unintentionally cut tissue prior to the user deploying the blade.
Jun 26, 2019	Z-2222-2019	—	terminated	There was a higher than normal incidence rate of the blade not retracting when tightening.
Apr 19, 2018	Z-2107-2018	—	terminated	The Instructions for Use (IFU) is incorrect with regards to sterilization parameters and must be replaced.
May 22, 2017	Z-0412-2018	—	terminated	One lot was found to contain both the correct twist drill (1.6mm) as well as an incorrect twist drill (2.0mm)
Feb 21, 2017	Z-1407-2017	—	terminated	Mislabeling on three lots of K-Wires. The incorrect product description " dual trocar" instead of "single trocar" was on the product label on the following parts: 1600-9355NS (lot 61005), 1600-9625NS (lot 60297), and 1604-162NS (lot 62856).
May 6, 2016	Z-2294-2016	—	terminated	MicroAire has initiated a limited recall (29 Units)on the Endotine Transbleph 3.5 (CFD-080-0167), Lot # 285373, due to minor mislabeling ( the front label is correct, but the side label lists an incorrect part number, i.e. CFD-080-0177).
Mar 11, 2016	Z-1834-2016	—	terminated	MicroAire discovered that 20 suspect Impactor instruments ( MicroAire Pneumatic Impactor) were shipped to end users and were missing the lock and unlock symbol markings on them.
Feb 8, 2016	Z-1328-2016	—	terminated	MicroAire has initiated a recall on product PAL-R4011XL (40cm x 4mm Del Vecchio French Rasp cannula), due to our receipt of three (3) complaints that it bent or broke during surgery. Accordingly, the PAL-R4011XL has also been put on production hold until further notice.
Feb 8, 2016	Z-1323-2016	—	terminated	Complaints that the cannula bent/broke during surgery.
Jun 12, 2015	Z-2821-2015	—	terminated	There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.
Jun 12, 2015	Z-2822-2015	—	terminated	There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.
Aug 12, 2013	Z-2159-2013	—	terminated	A medical device used in surgical procedures was packaged in a pouch in which a defective seal may compromise sterility
Aug 12, 2013	Z-2158-2013	—	terminated	A medical device used in surgical procedures was packaged in a pouch in which a defective seal may compromise sterility
Apr 26, 2012	Z-1792-2012	—	terminated	Medical device was not manufactured under Good Manufacturing Procedures and a user may be unable to sterilize the device according to procedures.
Sep 23, 2003	Z-0043-04	—	terminated	Wiring pin locking mechanism defective, potential to come apart in surgical site.
Sep 23, 2003	Z-0044-04	—	terminated	Wiring pin locking mechanism defective, potential to come apart in surgical site.