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Symmetry Penfield 65-1016

by Aspen Surgical Products, Inc.

Symmetry Penfield 65-1016 is a Class I device made by Aspen Surgical Products, Inc., listed in FDA GUDID since 2 Aug 2024 (UDI-DI 00887482025253), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00887482025253 UDI-DI Date2 Aug 2024ListedStatusListed 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  • Withdrawn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
Symmetry Penfield
Generic name
Open-surgery dissector
Model / reference
65-1016
Primary DI / UDI-DI
00887482025253
FDA product code
GDI
GMDN term
Open-surgery dissector
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 7.75 Inch

Related devices

Category: Open-surgery dissector

Similar devices in this category

Other devices filed under Open-surgery dissector.

Other devices from Aspen Surgical Products, Inc.

See all devices from Aspen Surgical Products, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)