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MicroAire® ZO-7163

by MicroAire Surgical Instruments LLC

MicroAire® ZO-7163 is a Class I device made by MicroAire Surgical Instruments LLC, listed in FDA GUDID since 17 Sep 2022 (UDI-DI 00847399013880), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00847399013880 UDI-DI Date17 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
MicroAire®
Generic name
Surgical saw blade, oscillating, single-use
Model / reference
ZO-7163
Primary DI / UDI-DI
00847399013880
FDA product code
GES
GMDN term
Surgical saw blade, oscillating, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Size
Width — 25.4 Millimeter
Length — 90 Millimeter

Related devices

Category: Surgical saw blade, oscillating, single-use

Other devices from MicroAire Surgical Instruments LLC

See all devices from MicroAire Surgical Instruments LLC →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)