FDA Registration Active 🇺🇸 United States

RENOVO, INC.

Reg #: 3014023545 · FEI: 3014023545 · Expires 2026
Products
27
Proprietary Names
5
Establishment Types
1
Classifications
27

Registration Details

Registration Name
RENOVO, INC.
Registration Number
3014023545
FEI Number
3014023545
Status
Active
Expiry Year
2026
Initial Importer
No
Address
340 SW COLUMBIA ST
City
Bend
State
OR
ZIP
97702
Country
US

Regulatory Submissions

510(k) Number
K172092

Owner / Operator

Firm Name
ReNovo, Inc
Operator Number
10054580
Address
340 SW Columbia St
City
Bend
State
OR
Postal Code
97702
Country
US
Correspondent
Mark Wells

Products

Device Name Product Code
Awl HWJ
Punch, Surgical LRY
Bone Mill LYS
Blade, Saw, General & Plastic Surgery, Surgical GFA
Accessories, Arthroscopic NBH
Blade, Scalpel GES
Bur, Ear, Nose And Throat EQJ
Orthopedic Manual Surgical Instrument LXH
Bit, Drill HTW
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment HWE
Tourniquet, Pneumatic KCY
Instrument, Surgical, Disposable KDC
Passer HWQ
Rasp HTR
Bur, Surgical, General & Plastic Surgery GFF
Arthroscope HRX
Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed NUJ
Staple, Removable (Skin) GDT
Passer, Wire, Orthopedic HXI
Countersink HWW
Burr, Orthopedic HTT
Laparoscope, General & Plastic Surgery, Reprocessed NLM
Retractor GAD
Stylet, Surgical, General & Plastic Surgery GAH
Electrosurgical, Cutting & Coagulation & Accessories GEI
Reamer HTO
Laryngoscope, Rigid CCW

Proprietary Names

ReNovo, Inc. ENT Shaver/Abrader Renovo, Inc. ReNovo,Inc. ReNovo Inc.

Establishment Types

Reprocess Single-Use Device